Job Openings

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Accounting Specialist III Performs daily accounts payable responsibilities, ensuring that all accounts payable documents are properly coded, authorized, and entered for payment. The position works under the supervision of the Accounts Payable Managers. The specialist performs daily responsibilities independently, though in a team environment, and uses initiative and judgment in investigating and resolving accounts payable discrepancies following established guidelines.

Responsibilities

• Using Hyland AnyDoc and OnBase software, prepare vendor invoices for payment, verifying product, price, quantity, and extensions on invoices, ensuring purchase order limits are not exceeded and all items submitted for payment are properly authorized, and initiating corrective actions as necessary
• Communicate tax status with vendors. Make conscious and correct decision about taxability of product
• Reconcile vendor statements to company records, investigating discrepancies and initiating corrections within department guidelines as necessary
• Communicate with end users by phone and/or email to assist with any payment issues
• Communicate with vendors by phone and/or email to reconcile accounts as well as educate vendors regarding Fred Hutch tax status
• Audit check and ACH payments prior to mailing
• Assist with ProCard auditing
• Perform other duties as assigned

Qualifications

• High school graduation or GED
• Minimum of three years accounts payable experience
• Experience with Washington State sales/use tax regulations
• Proficient with Microsoft Office Suite
• Excellent oral and written communication skills
• Well organized with attention to detail
• Experience with automated accounts payable systems
• Hyland OnBase and PeopleSoft AP experience advantageous

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The SCCA Administrative Fellowship Program offers early careerists an opportunity to develop their leadership style and to use their skills and competencies at one of the top 10 cancer programs in the nation, and the top ranked cancer hospital in the WWAMIO region. The fellow will be placed in Service Line Management, the strategy and business development arm of the institution, giving the fellow exposure across the care continuum and experience with executive and clinical leadership. Project-based in nature, the fellowship enables the fellow and the designated preceptor to determine the appropriate project portfolio through a concentration option that ensures a learning environment and the ability to translate academic theory into practice. The program is one year in length and aims to identify and grow promising candidates for future leadership positions.

Applications will be accepted from Aug. 1 through September 30th.

Learn more about the Administrative Fellowship at SCCA's website.

Responsibilities

The fellowship offers a rotation-based experience with projects geared towards the fellow’s interests and needs of the enterprise. This structure aims to provide a well-rounded understanding of the organization and disease-specific programs. Service line exposure may include Blood and Marrow Transplant, Breast, Gastrointestinal, Genitourinary, Head and Neck, Immunotherapy, Heme/Heme Malignancies, Melanoma/Skin, Phase I, Renal, Sarcoma and Thoracic Programs.

As the Service Line Manager role spans organizations and departments, the fellowship offers an opportunity to work on initiatives cross-institutional and cross-departmental in nature. The fellow is exposed to different managerial and leadership styles, helping to promote development and understanding of their own personal style.

Qualifications

Education
Applicants must have received or be expected to receive an MHA, MPH, MBA or similar master’s degree in a related field of study from an accredited graduate program prior to expected start date.

Skills & Qualifications

• Health care experience (preferably within a health care system)
• Strong academic record
• Strong communication skills (both oral and written)
• Ability to work on multiple projects at once
• Ability to be flexible, intuitive and inventive
• Self-motivated and team oriented
• Conducts self in a professional manner
• A keen desire to learn and grow as a leader in healthcare.

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

Seattle Cancer Care Alliance is an AAPA CHLM Employer of Excellence. We offer great generous benefits, including relocation and tuition reimbursement.

The ARNP/PA-C is a certified physician assistant or advanced registered nurse practitioner who provides evaluation and medical management of Breast Oncology patients at the Seattle Cancer Care Alliance. They follow patients during their chemotherapy and provide medical supportive care, as well as surveillance after completion of treatment. This position also provides opportunities for autonomous practice within the Women’s Wellness Follow-up Clinic, a long- term survivor and high risk clinic. The ARNP/PA-C assesses and manages basic health needs of patients, addresses treatment toxicities, performs procedures, monitors for cancer progression or recurrence, and consults with professional peers as needed. They work collaboratively with the treatment team to coordinate care of their patients. All clinical responsibilities are performed within the scope of practice, institutional privileges and under the supervision of an attending physician.

Responsibilities

Qualifications

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

Seattle Cancer Care Alliance is an AAPA CHLM Employer of Excellence. We offer great generous benefits, including relocation and tuition reimbursement.

Responsibilities

A Seattle Cancer Care Alliance ARNP/PA-C is a certified physician assistant or advanced registered nurse practitioner who provides evaluation and medical management to patients at the Seattle Cancer Care Alliance. This Full Time Advanced Practice Provider (ARNP or PA-C) will work with our General Oncology and Supportive Care Services in a “float” capacity. This will include management and coordination of clinical & research care under the supervision of an Attending Physician including, but not limited to, Lung, Head and Neck, GI, GU, Breast, and Sarcoma. Position responsibilities include but are not limited to:

• following patients during their chemotherapy and providing medical supportive care
• addressing and managing treatment toxicities
• monitoring for cancer progression or recurrence
• consulting with professional peers as needed
• working collaboratively with the treatment team to coordinate care of their patients
• actively participating in the conduct of cancer clinical research, including patient, caregiver, and peer education
• collaborating and consulting with other disciplines and services to ensure safe, effective, and timely treatment as well as continuity of patient care
• coordinating care in a multidisciplinary fashion with collaborating services which may include surgery, radiation oncology, medical oncology, nutrition, social work, psychology, pain service, hospice, and palliative care.
• all clinical responsibilities are performed within the scope of practice, institutional privileges and under the supervision of an attending physician

Qualifications

• 2 years of ARNP or PA-C experience in Medical Oncology required.
• Strong team player with a can-do attitude is a must! Self-directed and driven, with the ability to work as part of a multi-disciplinary team essential to the success of the person in this position.
• Graduate of an accredited Physician Assistant or Nurse Practitioner program required.
• ACLS, Washington state & DEA licensure required.
• Strong oral and written communication skills required.
• EMR experience required; prefer experience with CPOE

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

Seattle Cancer Care Alliance is an AAPA CHLM Employer of Excellence. We offer great generous benefits, including relocation and tuition reimbursement.

A Seattle Cancer Care Alliance ARNP/PA-C is a certified Advanced Registered Nurse Practitioner or Physician Assistant who provides evaluation and medical management of GU Oncology patients at the Seattle Cancer Care Alliance. They follow patients during and after their treatment course which may include chemotherapy, a research protocol or surveillance. The ARNP/PA-C assesses and manages basic health needs of patients, addresses treatment toxicities, monitors for cancer progression or recurrence, and consults with other members of the care team as needed. All clinical responsibilities are performed within the scope of practice, institutional privileges, and under the supervision of an attending physician.

Responsibilities

• Performs complex and problem-focused H & P’s
• Evaluates and manages on-treatment and post-treatment side effects, as well as long-term surveillance and survivorship issues.
• Manages issues associated with lines (PICC, PORT) and tubes (foley catheter, suprapubic and nephrostomy tubes)
• Collaborates and consults with other disciplines and services to ensure safe, effective, and timely treatment as well as continuity of patient care with both outpatient and inpatient teams.
• Participates in the conduct of all phases of cancer clinical trials or research protocols.
• Provides patient, caregiver, and peer education and support
• Helps to mentor GU team members (RN, MA, TC, research coordinators)
• Participates in GU clinical team and research meetings, conferences and committees
• Active member of the SCCA Rapid Response/Code Team (responsible to cover 4 weeks every year)
• Opportunity to participate in CPI projects with GU team and Medical Director

Qualifications

• One or more year(s) of ARNP or PA-C experience in Medical Oncology preferred.
• Strong team player with a can-do attitude is a must! Ability to work as part of a multi-disciplinary team.
• Graduate of an accredited Nurse Practitioner or Physician Assistant program required.
• Washington state & DEA licensure required.
• ACLS required (may obtain after hire).
• Strong oral and written communication skills required.
• EMR experience required

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

Seattle Cancer Care Alliance is an AAPA CHLM Employer of Excellence. We offer great generous benefits, including relocation and tuition reimbursement.

The ARNP/PA-C is a certified physician assistant or advanced registered nurse practitioner who provides evaluation and medical management of Heme/Heme Malignancy patients (primarily acute leukemias) at the Seattle Cancer Care Alliance. They follow patients during their chemotherapy and provide medical supportive care, as well as surveillance after completion of treatment. The ARNP/PA-C assesses and manages basic health needs of patients, addresses treatment toxicities, performs procedures, monitors for cancer progression or recurrence, and consults with professional peers as needed. They work collaboratively with the treatment team to coordinate care of their patients. All clinical responsibilities are performed within the scope of practice, institutional privileges and under the supervision of an attending physician.

Responsibilities

• Performs complex and problem-focused H & P’s

• Evaluates and manages on-treatment and post-treatment side effects, as well as long-term surveillance and survivorship issues.

• Performs procedures (bone marrow aspiration and biopsy, lumbar puncture with intrathecal chemotherapy, etc.) according to licensure, credentialing, and scope of practice

• Collaborates and consults with other disciplines and services to ensure safe, effective, and timely treatment as well as continuity of patient care.

• Participates in the conduct of cancer clinical research

• Provides patient, caregiver, and peer education

• Communicates effectively with inpatient and outpatient teams

• Participates in patient rounds, conferences and committees

• Active member of the SCCA Rapid Response/Code Team

Qualifications

• 1 year of ARNP or PA-C experience in Medical Oncology
• Strong team player with a can-do attitude is a must! Ability to work as part of a multi-disciplinary team is essential.
• Graduate of an accredited Physician Assistant or Nurse Practitioner program required.
• Washington state & DEA licensure required.
• ACLS required
• Strong oral and written communication skills required.
• EMR experience required; prefer experience with CPOE

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

Seattle Cancer Care Alliance is an AAPA CHLM Employer of Excellence. We offer great generous benefits, including relocation and tuition reimbursement.

Responsibilities

This full time Advanced Practice Provider (ARNP or PA-C) will work at our satellite clinic in Poulsbo, Washington. They will actively coordinate the complex care of cancer patients undergoing both systemic anti-cancer therapy and radiation therapy. The incumbent will manage side-effects of these therapies, order appropriate laboratory and radiographic studies; prescribe medications and refer patient to other specialists as necessary. The incumbent may provide for post-treatment cancer patients follow-up visits for the medically indicated period after completion of treatment. The incumbent will also provide psychological support to patients by participating in patient and/or family teaching and refer patients to community agencies and other resources to promote optimal adjustment and functioning.

This position requires the ability to lead other clinical staff, be accountable for the work required in this position, the ability to be flexible in a dynamic environment, and the relentless pursuit of excellent patient centered care. This clinic provides a broad range of services including GI, Lung, GU, Breast, and Hematologic Malignancies and Radiation therapy.

Qualifications

• 1 year of ARNP or PA-C experience in Medical Oncology
• Strong team player with a can-do attitude is a must! Ability to work as part of a multi-disciplinary team is essential
• Graduate of an accredited Physician Assistant or Nurse Practitioner program required
• Washington state & DEA licensure required
• ACLS required
• Strong verbal and written communication skills required
• EMR experience required; prefer experience with CPOE

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

Seattle Cancer Care Alliance is an AAPA CHLM Employer of Excellence. We offer great generous benefits, including relocation and tuition reimbursement.

A Seattle Cancer Care Alliance ARNP/PA-C is a certified physician assistant or advanced registered nurse practitioner who provides evaluation and medical management of Sarcoma oncology patients at the Seattle Cancer Care Alliance. They follow patients during their chemotherapy and provide medical supportive care, as well as surveillance after completion of treatment. The ARNP/PA-C assesses and manages basic health needs of patients, addresses treatment toxicities, performs procedures, monitors for cancer progression or recurrence, and consults with professional peers as needed. They work collaboratively with the treatment team to coordinate care of their patients. All clinical responsibilities are performed within the scope of practice, institutional privileges and under the supervision of an attending physician.

Responsibilities

• Performs complex and problem-focused H & P’s
• Evaluates and manages on-treatment and post-treatment side effects, as well as long-term surveillance and survivorship issues
• Performs procedures according to licensure, credentialing, and scope of practice
• Collaborates and consults with other disciplines and services to ensure safe, effective, and timely treatment as well as continuity of patient care
• Participates in the conduct of cancer clinical research
• Provides patient, caregiver, and peer education
• Communicates effectively with inpatient and outpatient teams
• Participates in patient rounds, conferences and committees
• Active member of the SCCA Rapid Response/Code Team

Qualifications

• One year of ARNP or PA-C experience in Medical Oncology required
• Strong team player with a can-do attitude is a must! Ability to work as part of a multi-disciplinary team is essential
• Graduate of an accredited Physician Assistant or Nurse Practitioner program required
• Washington state & DEA licensure required
• ACLS required
• Strong oral and written communication skills required
• EMR experience required; prefer experience with CPOE

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

Responsibilities

The Advanced Practice Provider (APP) provides care for blood and marrow transplant patients and immunotherapy patients in both the inpatient and outpatient settings under the supervision of the attending physician.  The APP is responsible for the primary care of the patient to include assessment, triage and management of the transplant patient as part of a collaborative transplant team.  Responsibilities include obtain medical history, perform physical examinations, review and order diagnostic studies, radiographs and prescribe treatments.  APPs perform bone marrow aspirations, lumbar punctures and are first assists with Bone Marrow Harvests and provide follow-up care of bone marrow donors under the supervision of attending physician.

Qualifications

• Must be a graduate of a Physician Assistant training program or appropriate Nurse Practitioner program and be able to practice in the state of Washington (licensed). 
• Have National Certification as appropriate for profession
• Must be licensed for schedule II drug authority. 
• Strong oral and written communication skills required. 
• Basic computer skills are essential. 
• Must be able to work as part of a multi-disciplinary team. 
• Must enjoy long-term relationships with patients undergoing intense therapy. 
• Oncology or BMT experience preferred.

Please include a cover letter when applying for this job that includes your specific interest in the Advanced Practice Provider position and working for Fred Hutch (either as an additional attachment on your profile or merged into the file that contains your resume.)

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

We offer great generous benefits, including relocation and tuition reimbursement.

The position will provide care to post-treatment patients in the SCCA Survivorship Clinic and provide care across the continuum from diagnosis to survivorship focused follow-up for patients in the SCCA Sarcoma Clinic.

Allocation of FTE: 50% survivorship, 25% sarcoma survivorship, 25% general sarcoma care. 

SCOPE OF RESPONSIBILITY

Within the Survivorship Clinic the Nurse Practitioner/Physician Assistant will be responsible for provision of clinical care and patient education for a broad range of cancer survivors, including  adult survivors of pediatric cancers.  S/he will work with a comprehensive team including the program director and co-director, the program nurse coordinator, and the program manager toward the goal of extending survivorship services to all oncology patients, regardless of age, place or type of treatment. S/he will collaborate with other providers within the Survivorship Clinic, within other SCCA oncology discipline clinics, and also with physicians and other health care professionals to define best practices of care, develop comprehensive survivorship care guidelines, and establish referral networks internal and external to the SCCA.

Within the Sarcoma Clinic the Nurse Practitioner/Physician Assistant will provide evaluation and medical management of Sarcoma patients at the Seattle Cancer Care Alliance.  They will follow patients during their chemotherapy and provide medical supportive care, as well as surveillance. The ARNP/PA-C assesses and manages basic health needs of patients, addresses treatment toxicities, performs procedures, monitors for cancer progression or recurrence, and consults with professional peers as needed.  They work collaboratively with the treatment team to coordinate care of their patients. The clinician in this role will be expected to see patients along the continuum of care for sarcoma patients, including long term follow-up of sarcoma survivors in the Survivorship clinic conducting survivorship focused visits as described below as well as carrying out surveillance plans following standard treatment pathways in collaboration with the sarcoma medical oncologists. 

Responsibilities

Survivorship Program: Comprehensive onsite evaluations for cancer survivors including:

• Review of diagnosis, treatment, acute and chronic complications and co-morbidities
• Risk-adapted history and physical examination, laboratory and diagnostic studies
• Psychosocial and functional needs assessment
• Referral to appropriate subspecialties and services
• Preparation of treatment summary or review of treatment summary developed by survivorship RN, including guidelines and recommendations for follow-up
• Patient education
• Provide written (and oral when necessary) communication of survivors evaluation back to referring provider and/or primary care provider
• Other Duties as assigned by program director or program manager:
  • Participate in program outreach activities (e.g. local or regional presentations regarding survivorship, or the survivorship program survivor education conferences, and other related activities), including off-hours as necessary
  • Participate in program development activities (e.g. visits to internal or off-site clinics or hospitals, and other related activities, development of standard of care guidelines)
  • Develop educational materials for survivors (e.g. Survivor notebook, health links, etc.)
  • Create, review and maintain accuracy and completeness of survivorship database care plan recommendations  

Sarcoma Clinic:

• Performs complex and problem-focused evaluation and management for patients diagnosed with Sarcoma
• Evaluates and manages on-treatment and post-treatment side effects, as well as long- term surveillance.
• Performs procedures according to licensure, credentialing, and scope of practice
• Collaborates and consults with other disciplines and services to ensure safe, effective, and timely treatment as well as continuity of patient care.
• Participates in the conduct of cancer clinical research
• Provides patient, caregiver, and peer education
• Communicates effectively with inpatient and outpatient teams
• Participates in patient rounds, conferences and committees
• Active member of the SCCA Rapid Response/Code Team

PROFESSIONAL CONDUCT

Employees within the Survivorship Program are expected to maintain high standards of professionalism in their interactions with patients, referring providers and other team members. Professional conduct includes:

• Fosters positive and professional interpersonal relationships with patients, families, staff, referring physicians and other visitors.
• Actively promotes positive working relationships within survivorship team and all SCCA, FHCRC and UWMC staff to create an affirming work environment.
• Is flexible and positive in accepting other duties or projects as assigned by the program director or program manager.
• Identifies and reports barriers to clinical and departmental effectiveness and facilitates/ suggests effective problem solving.
• Seeks positive resolution of interpersonal conflicts though self-awareness, mutual respect and skillful communication.
• Is aware of and follows policy and procedures regarding infection control, health, safety and security.
• Adheres to survivorship team and FHCRC, SCCA and departmental personnel policies including attendance, punctuality, and timekeeping standards.
• Supports FHCRC and the SCCA in its efforts to fulfill its mission.

Qualifications

• 1 year of ARNP or PA-C experience in Medical Oncology or BMT required
• Strong team player with a can-do attitude is a must! Ability to work as part of a multi-disciplinary team is essential.
• Graduate of an accredited Physician Assistant or Nurse Practitioner program required.
• Washington state & DEA licensure required.
• ACLS required
• Strong oral and written communication skills required.
• EMR experience required; prefer experience with CPOE

PAY, BENEFITS & WORK SCHEDULE

• Salary DOE + excellent benefits; 1.0 FTE position. Will require some evening hours.

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

Under the oversight of the Strategy Division, the Strategic Outreach and Affiliate Network Office oversees an array of responsibilities in the service of Seattle Cancer Care Alliance’s goal of improving cancer care, regionally and beyond. We strive to further the reach of the SCCA’s expertise and knowledge by developing new relationships through local, regional and international events and conferences as well as maintain and cultivate deeper relationships with our existing partners. The Affiliate Network brings community cancer care centers together to help support SCCA's mission and provide the latest treatment information to patients seen in the community. The outreach component of the department’s responsibilities provide community-based physicians educational programs, targeted to specific disease sites focusing on advancements to diagnostic techniques and treatment modalities.

Under the general direction of the Strategic Outreach and Affiliate Network Director and Medical Director, the Affiliate Network Program Manager will lead, manage and execute projects for the SCCA affiliate network program, impacting multiple organizations and departments. This position requires Strategic Leadership, Complex Decision Making, Relationship Management, and Project Management skills, bringing together external partners and internal stakeholders in support of SCCA's mission to advance oncology care and research, regionally and beyond.

Responsibilities

Relationship Management

• Serves as key point of contact between members of the SCCA’s Affiliate Network and the SCCA, along with its founding institutions UW Medicine, Fred Hutch and Seattle Children’s.
• Foster strong relations with affiliate sites, serving SCCA’s mission of advancing care and improving outcomes for patients regionally and beyond.
• Plan and participate in affiliate-based activities and outreach events, aligned with SCCA strategic growth goals.
• Travel to network sites at least monthly (25%)

Project Management 

• Plan and conduct annual strategic retreats with each network site to identify initiatives and agree on goals related to network program components: education, program development, quality, research, community engagement, and increased access to resources at SCCA and its partners.
• Project Manager to a cross functional team at SCCA, the Network Collaborative Workgroup. This group of clinical experts, research, operations, intake, quality and marketing stakeholders, work together to track, report on and resolve issues in support of SCCA’s commitments to affiliate members.
• Hold monthly conference calls with network affiliates to facilitate programmatic work, manage projects and next steps.
• Set goals, track and monitor progress using project management approach, providing regular updates to Director, Medical Director, stakeholders, and SCCA clinical and administrative leaders.
• Responsible for managing Affiliate Network Budget and allocating resources appropriately between sites.

Strategic Leadership and Complex Decision Making

• Develop and maintain knowledge of critical healthcare policy, research and other oncology events that could impact scientific, regulatory or clinical practice for affiliate member sites. Develop program offerings responding to those impacts. 
• Research, conceptualize, propose and continuously improve program components and services to grow and strengthen the Network Affiliate Program.
• Provide project management leadership support to department director to refresh program support materials and external offerings.
• Conceptualize and develop online or digital forums for network members to share best practices among each other.
• Identify, facilitate and develop marketing and community engagement activities for affiliate events by collaborating with the marketing team.
• Under the guidance of the director, create communications plan to raise awareness and support for the Affiliate Network Program.
• Participate in cross-institutional projects including researching and compiling information as well as writing and editing content for external audiences.

Qualifications

• Bachelor’s degree with 5 years of progressively complex administrative and project management experience.
• Preferred Master’s degree in business, healthcare, Public Health, or an advanced clinical degree.
• Experience in a clinical oncology setting preferred.
• Business & Management: previous health administration, clinical, operational, or business management experience strongly preferred.
• Critical thinking skills: attention to detail required and an ability to use sound personal judgment and trouble shoot issues.
• Systems thinking: ability to understand the flow of a process, how all pieces fit together, and how making a change will impact the entire system.
• Facilitation: ability to increase the likelihood, strength, or effectiveness of the outcome of a diverse group. Ability to work vertically and horizontally. Excellent interpersonal skills and ability to work with a diverse group of external and internal stakeholders in a diplomatic manner.
• Strong written and verbal communication skills and proficiency with Microsoft Office applications required. Experience with Tableau Data Software and SharePoint preferred.
• Ability to prioritize work while managing multiple projects with competing timelines.
• Self-motivated team leader with energy and enthusiasm for improving team processes.
• Must have a valid Washington Driver’s license: frequent local and regional travel is required for this position.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first and largest cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Animal Equipment Preparer I processes soiled animal housing equipment and prepares clean equipment for use; performs general custodial care for areas within the facility; and may assist with inventory assessment checks for equipment supplies.

Responsibilities

• Prepare items for the equipment washers, including removal of soiled bedding, sorting of items into similar batches, soaking designated items and scrubbing items that are especially soiled.
• Preform housekeeping duties such as sweeping, mopping and garbage removal. 
• Learn all PPE policies and procedures throughout the small animal vivarium.
• Mix and use cleaning solutions appropriately.
• Operate equipment washers, automatic water bottle filling systems and autoclaves.
• Learn to perform environmental control tests to insure proper function. Learn to maintain records of test results as indicated by supervisory personnel. 
• Ensure that clean equipment has been processed correctly and shows no sign of residual waste material or other types of contamination. Become proficient at notifying the Lead of any damaged equipment. 
• Participate in material management inventory control, notifying supervisory staff of items that need to be ordered. 
• May participate in the transportation of items between the facilities.
• Attend and participate in assigned training classes.
• Perform other duties as assigned.

Qualifications

Minimum qualifications:

• Have sufficient verbal and written communication skills to be able to follow written and verbal instructions and assimilate training
• Ability to lift and move 50 lbs on a regular basis and sustained physical activities such as bending, balancing, stooping, reaching, and remain standing for long periods of time.
• Ability to wear Personal Protective Equipment including scrubs, gloves, shoe covers, gowns, ear plugs / muffs, face mask, and eye protection.

Preferred qualifications:

• High school diploma or equivalent.
• Maintenance of a valid Washington State Driver’s License and good driving record

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first and largest cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Animal Equipment Preparer I processes soiled animal housing equipment and prepares clean equipment for use; performs general custodial care for areas within the facility; and may assist with inventory assessment checks for equipment supplies.

Responsibilities

• Prepare items for the equipment washers, including removal of soiled bedding, sorting of items into similar batches, soaking designated items and scrubbing items that are especially soiled.
• Preform housekeeping duties such as sweeping, mopping and garbage removal. 
• Learn all PPE policies and procedures throughout the small animal vivarium.
• Mix and use cleaning solutions appropriately. Operate equipment washers, automatic water bottle filling systems and autoclaves. Learn to perform environmental control tests to insure proper function. Learn to maintain records of test results as indicated by supervisory personnel. 
• Ensure that clean equipment has been processed correctly and shows no sign of residual waste material or other types of contamination. Become proficient at notifying the Lead of any damaged equipment. 
• Participate in material management inventory control, notifying supervisory staff of items that need to be ordered. 
• May participate in the transportation of items between the facilities.
• Attend and participate in assigned training classes.
• Perform other duties as assigned.

Qualifications

Minimum qualifications:

• Have sufficient verbal and written  communication skills to be able to follow written and verbal instructions and assimilate training
• Ability to lift and move 50 lbs on a regular basis and sustained physical activities such as bending, balancing, stooping, reaching, and remain standing for long periods of time.
• Ability to wear Personal Protective Equipment including scrubs, gloves, shoe covers, gowns, ear plugs / muffs, face mask, and eye protection.

Preferred qualifications:

• High school diploma or equivalent
• Maintenance of a valid Washington State Driver’s License and good driving record

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Assistant Research Tech is responsible for supporting the small animal imaging needs of researchers and Comparative Medicine at Fred Hutch. The specialist will assist the researchers in the use of multiple imaging equipment (including Ultrasound, MRI, Optical imaging equipment), provide imaging services and extend support to small animal clinical services when needed. This position will be expected to operate specialized equipment and to perform specialized procedures as required to support animal manipulation segments of research protocols. Completion of these tasks will be expected to be conducted independently without direct supervision. A clear understanding of research protocols is required.

Responsibilities

• Work to provide excellent customer service and quality images and data for research staff.
• Become proficient using multiple imaging modalities, including radiography, MRI, ultrasound and bio-luminescence.
• Perform imaging studies including animal preparation, anesthesia, physiologic monitoring, placement, completion of imaging protocols, and compilation of data for investigators.
• Become proficient in multiple clinical procedures including (but not limited to) anesthesia, injections, surgical procedures, specimen collections, treatment administration.
• Coordinate and complete research clinical service requests.
• Coordinate and complete maintenance on imaging equipment and software.
• Follow safe animal and equipment handling guidelines and SOPs.
• Develop SOPs, training aids, and guidelines for clinical services and use of imaging equipment.
• Develop and facilitate training and education sessions for use and maintenance of imaging equipment.
• Coordinate and support transportation of animals across facilities for imaging related research.
• Establish and maintain positive, collaborative working relationships with faculty in order to provide high quality customer service.
• Work closely with research staff to identify needs and develop service solutions.
• Become cross-trained in order to serve as back-up for other CM services and organizational staff as needed.
• Complete duties effectively and efficiently with little or no supervision.
• Work on call, weekend, evening, or holiday shifts as needed or assigned.
• Other duties as assigned.

Qualifications

Minimum qualifications:

• Bachelor’s degree or equivalent combination of experience and education.
• Excellent communication and organizational skills.
• Demonstrated ability to learn and adapt to new systems and techniques.
• Basic understanding of translational research using in vivo models.
• Maintenance of a valid Washington State Driver’s License and good driving record.

Preferred qualifications:

• Experience in performing research using murine models
• Experience in handling and using imaging modalities including MRI, ultrasound, optical imaging etc.
• AALAS certification at the LAT level is recommended, and persons hired for this position should continue to pursue this certification as soon as possible once eligible until achieved.

Overview

**Please note that this requisition is for an upcoming opportunity which we are proactively seeking interested candidates**

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first and largest cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Animal Technician I-III performs routine rodent husbandry, custodial care for the rodent areas, and processes equipment. The Technician I-III position is overseen by the Animal Technician Lead and is a direct report to the Animal Technician Manager.  This is considered an entry level position for individuals with no prior experience in laboratory animal care procedures or skilled individuals who are transitioning from other animal care positions. The position of tech I-III will be determined depending on experience.

Responsibilities

• Learn to and become proficient in providing care for all small animal species on a daily basis in accordance with standard operating procedures. Learn to evaluate animals’ general health, report abnormalities to the small animal veterinary technologist or veterinarian for veterinary evaluation. Learn to perform preventive animal health care duties and administer treatments as prescribed.
• Learn to and become proficient in providing feed to animals according to prescribed SOPs and insure that animals have fresh water at all times.
• Learn to and become proficient in changing animal housing according to schedule by transferring animals to clean housing and transporting soiled housing and accessories to the wash area.
• Learn to and become proficient in performing housekeeping duties such as sweeping, mopping, garbage removal, and equipment washing in animal housing areas and surrounding premises.
• Learn to and become proficient in maintaining accurate records of animal identification, veterinary treatments, animal census, facility housekeeping, and room parameters (e.g. daily temperature high and low).
• Learn to and become proficient in effectively communicating with research staff regarding the status of their animals through verbal, written, or electronic means.
• Learn to and become proficient in using and maintaining animal housing IVC systems and hoods, including routine cleaning, checking air flow gauges, attaching and removing blower units, securing hoses, and relocating racks to the cage wash facility for sanitizing.
• Learn to and become proficient in PPE policies and procedures throughout the small animal vivarium.
• Learn to and become proficient in appropriately mix and use of all cleaning solutions according to established SOPs and/or manufacturers’ instructions.
• Learn to and become proficient in operation of equipment washers, automatic water bottle filling systems and autoclaves under supervision.
• Learn to and become proficient in material management inventory control, notifying the supervisor or designated technicians of items that need to be ordered.
• Attend and participate in assigned training classes.
• May transport or assist in transport of animals, supplies or equipment between facilities or may assist in such activities.
• Work on call, weekend, evening, or holiday shifts as needed or as assigned.
• Perform other duties as assigned.

Qualifications

• High school diploma or equivalent.
• Good verbal and written communication skills.
• Ability to follow written and verbal instructions
  
• Ability to lift and move 50 lbs on a regular basis and sustained physical activities such as bending, balancing, stooping, reaching, and remain standing for long periods of time.  
• Ability to wear Personal Protective Equipment including scrubs, gloves, shoe covers, gowns, ear plugs / muffs, face mask, and eye protection.

Desired Qualifications

• Science and animal husbandry background. 

**Please note that this requisition is for an upcoming opportunity which we are proactively seeking interested candidates**

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Apprentice Engineer is responsible for performing independently or under supervision, tasks of a skilled nature, necessary for the operation, maintenance, repair, and remodeling of Center buildings, grounds and equipment. The incumbent must have an aptitude for mechanical, plumbing and refrigeration skills, and be able to obtain a class 3 boiler licenses. Additionally the incumbent should have working knowledge in at least two of the following areas: architectural, electrical, welding, HVAC, building automation, steam and hot water systems. This position reports to the Chief Engineer.

The engineer will be rotated through all departmental disciplines and perform work orders as assigned and be expected to complete them under supervision or independently depending on complexity of the work and completing all the required paperwork.

The engineer assists a skilled OE/Supervisor in all phases of work associated with a particular trade, and on occasion will be assigned relatively simple task to work independently. The individual should be able to complete the entire task which is assigned but should feel free to ask for additional instruction, guidance and oversight as needed. As the individual progresses through the apprentice program, these independent tasks will become more frequent and of a more complex nature commensurate with the level of skill the individual is displaying. The incumbent will be enrolled in a four-year supervised training program, with the employee progressing in 6 month increments if performance is satisfactory and license requirements, if any, are met. Responsibilities include:

1. Operates hand tools, power tools, and equipment relevant to selected trade.
2. Performs manual labor associated with the trade.
3. Runs errands, carries and delivers materials, tools and equipment.
4. Cleans tools and equipment.
5. Does skilled trades work commensurate with years of experience as apprentice.

The apprentice engineer will work the day shift Monday through Friday 6:30 AM to 3:00 PM and may be required to swing and or grave shift in accordance with the policies of the department.

The apprentice engineer will be required to enroll and complete the 4 year training program offered by Local 392, District 286. This will require a min of 8 hours of class time per week, which will be uncompensated by Fred Hutch, except to the extent outlined in the union contract.

Responsibilities

Type of work to be performed include the following under supervision. Other duties may be assigned.

• Performing General Physical Activities - Performing physical activities that require considerable use of your arms and legs and moving your whole body, such as climbing, lifting, balancing, walking, stooping, and handling of materials.
• Listens for unusual sounds from machines or equipment to detect malfunction and discusses machine operation variations with supervisors or other maintenance workers to diagnose problem or repair machine.
• Repairs and maintains plumbing by replacing washers in leaky faucets, mending burst pipes, and opening clogged drains.
• Dismantles defective machines and equipment and installs new or repaired parts.
• Cleans and lubricates shafts, bearings, gears, and other parts of machinery.
• Lays out, assembles, installs, and maintains pipe systems and related hydraulic and pneumatic equipment, and repairs and replaces gauges, valves, pressure regulators, and related equipment.
• Repairs and maintains physical structure of establishment.
• Opens valves on equipment such as compressors, pumps, and condensers to prepare system for operation and starts equipment and auxiliary machinery.
• Observes temperature, pressure and ampere readings for system and equipment and adjusts controls or overrides automatic controls to obtain specified operation of equipment.
• Makes periodic inspection of equipment and system to observe operating condition and need for repair or adjustment.
• Adjusts controls to isolate and clear broken lines for repair or shuts down equipment.
• Repacks pumps and compressors, cleans condensers, and replaces worn or defective parts.
• Replaces damaged ceiling tile, floor tile, and wall coverings.
• Visually inspects and tests machinery and equipment.

Qualifications

• High School diploma or equivalent
• Possess and maintain a valid Washington State Driver’s License
• Have a sound knowledge and understanding of using and handling equipment and tools
• Must be able to lift 50 lbs.
• Dependable, on-time and proven good work habits
• Good communications skills
• Able to work a varied schedule including shift work

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The HIV Vaccine Trials Network (HVTN) Laboratory Center is part of an international collaboration of scientists and educators searching for effective and safe vaccines. The HVTN’s mission is to facilitate the process of testing preventive vaccines against HIV/AIDS. The Laboratory Center has an annual budget of more than $25 million and employs approximately 200 employees throughout the program. The organization conducts all phases of clinical trials from evaluating experimental vaccines for safety and the ability to stimulate immune responses through to testing vaccine efficacy. The HVTN Laboratory Center is seeking an Research Finance Assistant Director.

The Research Finance Assistant Director is responsible for driving all activities related to financial planning, grants and contracts, bugeting and analysis for the HVTN Laboratory Center, related grants and Division activities. This position will report to Director of Program Operations, Immunology and Vaccine Development (IVD) Program and will be a valued consultant to the Senior Vice President and Director, VIDD/HVTN Principal Investigator. The position will drive the international grants and contracts, budget and planning process for the Laboratory Center, as well as perform financial analysis. This position will provide strategic direction for a long-range financial view of the grant life cycle and beyond, while taking into consideration internal and external variables and constraints. Significant experience in complex sponsored research projects and financial analysis as well as a demonstrated track record as a leader who values teamwork, collaboration and communication are critical for this role. The ability to effectively communicate financial complexities to a range of audiences is essential.

The Research Finance Assistant Director will also manage a small team and will leverage Division and organizational resources to accomplish goals. In addition, this position will work closely with HVTN Leadership Operations Center, HVTN Statistical Data Management Center, Finance and Accounting as well as across functions (Office of General Council, Business Development & Strategy, IT and Human Resources). The position requires an ability to direct and manage multiple priorities, quickly analyze situations and make sound decisions using effective time management skills, good business acumen, and administrative judgment.

Responsibilities

A. Financial Strategy and Operations

• Provide direction and support to the Senior Vice President and Director, VIDD/HVTN Principal Investigator, on the financial strategy and planning of the HVTN Laboratory Center and related activities.
• Develop and maintain key reports for reporting performance against the budget, internal and external requirements to drive accountability and transparency. Prepare information and reports that forecast trends, analyze performance results, and address financial concerns.
• Establish and drive the annual budget and planning process including communicating across HVTN programs and Center leadership.
• Oversee and monitor all grant and fiscal activities within the HVTN Laboratory Center Programs including all national and international sites. Establish and comply with financial requirements of NIH and/or the specific funding agency as well as Fred Hutch policies.
• Assist the Director of Program Operations-IVD and VIDD Senior Operations Director and in the development of short and long term planning of financial resource management, in monitoring spending levels on accounts, advising them of any change in spending status, and troubleshoot/resolve problems or questions regarding budgets.

B. Team Leadership

• Manage a small team of fiscal staff.
• Establish a regular cadence of HVTN Laboratory Center Financial meetings including the tracking and monitoring of agendas and action items.
• Serve as coordinator and contact between members, study investigators, oversight committee and working group leads on all financial matters.
• Serve as a special advisor to VIDD financial teams for financial management related to sponsored and non-sponsored finance, forecasting and best practice.  

C. Financial Reporting and scientific related visits/meetings

• Coordinate specific reports as requested by the Division of AIDS, NIH (DAIDS)
• Serve as the primary point of contact on all post-award financial activities for sponsor communications in coordination with the Principal Investigator.
• Oversee the submission of the annual progress report including budgets to DAIDS and related reports.
• Maintain communications and track fiscal team group progress. Communicate and track timelines and milestones.
• Create and maintain a system or executive report for portfolio financial reporting for the Senior Vice President and Director, VIDD/HVTN Principal Investigator that includes summary and detailed reports for each grant and active account.
• Develop reports and/or systems that forecast trends, analyze performance results, and address financial concerns.

D. Other Duties

• Continuously improve the budget and forecasting process and reports, including championing data structure and support.
• Assist with financial negotiations related to the Laboratory Center in partnership with Senior Vice President and Director, VIDD/HVTN Principal Investigator, Senior Operations Director, VIDD, Director of Program Operations-IVD, Business Development and Fred Hutch administration, upon request.
• Perform other related duties as assigned including, but not limited to, financial support related to complex agreements, Board reporting and related due diligence.

Qualifications

Minimum qualifications:

• Bachelor’s degree in Accounting, Finance or related field; MBA is preferred
• 7-10 years of progressively complex experience in research finance and/or administration of department financial processes and systems including a minimum of 5 years experience working with sponsored research (NIH required)
• Minimum three years experience leading a team including direct supervision of staff
• Advanced Excel modeling skills and proficient in MS Office Suite applications
• Excellent oral and written communication skills
• Experience with Tableau and related data presentation software
• Knowledge of NIH grant application procedures, budget monitoring, databases, and financial terms

Key skills and abilities

• Excellent attention to detail and the ability to work independently are essential to success in this position, as are good communication and organizational skills
• Ability to work under pressure, and maintain confidentiality
• Ability to prioritize multiple tasks, organize, and work both independently and as part of a team
• Excellent attention to detail and the ability to work independently are essential to success in this position, as are good communication and organizational skills
• Must be flexible and willing to work some evenings and weekends as needed

Assistant Faculty in Basic Sciences Division

Fred Hutchinson Cancer Research Center invites applications for an open faculty position at the Assistant Member level in the Division of Basic Sciences. We seek an exceptional laboratory scientist conducting fundamental research into mechanisms that regulate the basic biology of normal or cancer cells. Current faculty members investigate diverse areas of molecular, computational, cellular, developmental, evolutionary and structural biology, metabolism, virology and immunity. We utilize a broad range of experimental and computational approaches and model systems. Fred Hutch provides outstanding colleagues, a collegial atmosphere, and a wealth of resources to support junior faculty success. Graduate students are drawn from the outstanding Molecular and Cellular Biology graduate program at the University of Washington. Fred Hutch is located in a modern campus by Lake Union in Seattle, Washington, and is close to other non-profit research institutes and the University of Washington. See our website for further information https://www.fredhutch.org/en/research/divisions/basic-sciences-division.html.

For consideration, applicants must have a doctoral degree and a substantial record of achievement pre and post-doctoral. Women and minorities are particularly encouraged to apply. Application deadline: October 31, 2019.

At Fred Hutch, we believe that the innovation, collaboration, and rigor that result from diversity and inclusion are critical to our mission of eliminating cancer and related diseases. We seek faculty members who bring new ways of seeing the world and solving problems. Fred Hutch is committed to ensuring that all candidates hired for faculty appointments share our commitment to diversity and inclusion.

Interested candidates should submit a curriculum vitae, research statement that is up to two pages in length including figures, excluding references, three letters of recommendation and a diversity statement describing your past contributions to diversity, equity, and inclusion and your future plans for continuing these efforts as a faculty member (one page or less).

Hematopoietic Cell Transplant (HCT) and Immunotherapy (IMTX) Programs

The Fred Hutchinson Cancer Research Center (Fred Hutch) and the University of Washington (UW) Department of Medicine are jointly recruiting a full-time faculty member at the Assistant Member/Assistant Professor or Associate Member/Associate Professor level without tenure due to funding (WOT), commensurate with experience, in the Clinical Research Division of the Fred Hutch and the Division of Medical Oncology, Department of Medicine at the UW. This position has an annual service period of 12 months [July 1-June 30].  The Fred Hutch, home of three Nobel laureates, is an independent, nonprofit research institution dedicated to the development and advancement of biomedical research to eliminate cancer and other potentially fatal diseases. Recognized internationally for its pioneering work in bone-marrow transplantation and immunotherapy, Fred Hutch and the UW provide a unique environment for conducting translational research and clinical care. The Fred Hutch, in collaboration with its clinical and research partners, the University of Washington and Seattle Children’s, is a National Cancer Institute-designated comprehensive cancer center.

The primary appointment will be in the Clinical Research Division of Fred Hutch. The selected individual for the advertised position is expected to enhance our clinical care and clinical research programs in hematopoietic cell transplantation and immunotherapy. All clinical research interests will be considered however, there is a particular interest in applicants with demonstrated experience in the field of immunotherapy. Applicants with extensive research experience will also be considered. University of Washington faculty engage in teaching, research and service.

Anticipated start date January 2, 2019

The Fred Hutchinson Cancer Research Center (Fred Hutch) and the University of Washington (UW) invite exceptional candidates to apply for a full-time faculty appointment at the rank of Assistant Member/Assistant Professor or Associate Member/Associate Professor level, commensurate with experience, in the Clinician-Scholar pathway in the Clinical Research Division of the Fred Hutch and in the Department of Pathology at UW without tenure due to funding (WOT). Fred Hutch, home of three Nobel laureates, is an independent, nonprofit research institution dedicated to the development and advancement of biomedical research to eliminate cancer and other potentially fatal diseases. Recognized internationally for its pioneering work in bone-marrow transplantation and immunotherapy, Fred Hutch provides a unique environment for conducting translational research and clinical care. Fred Hutch, in collaboration with its clinical and research partners, the University of Washington, Seattle Childrens Hospital, and Seattle Cancer Care Alliance (SCCA) is a National Cancer Institute-designated comprehensive cancer center.

The selected individual is expected to enhance our clinical care and clinical research programs in anatomic pathology, with particular focus in hematopoietic cell transplantation and immunotherapy.  Based on qualifications, this position could entail a leadership role. We offer access to a highly collaborative and diverse research environment, modern laboratory space and state-of-the-art core facilities.  Research is a core priority at the Hutch and successful candidates will be expected to maintain an active clinical research interest, as demonstrated by peer reviewed publications.  The primary appointment will be in the Clinical Research Division of Fred Hutch with secondary appointment with the Department of Pathology at the University of Washington.

The Fred Hutchinson Cancer Research Center invites applications from scientists working in the area of prostate cancer research. Applicants will be considered at the rank of Assistant or Associate Faculty member, and we are seeking individuals who share our goals to advance an understanding of the biological basis of prostate cancer, and to translate findings to the clinic. This position will primarily support an office-based ‘dry-lab’ faculty member and research team, though limited ‘wet-lab’ space and attendant resources will be available. We will consider PhD, MD/PhD, or MD scientists working in areas that include, but are not limited to: the microenvironment, metastasis, systems biology, computational biology, the biology of therapeutic response/resistance, genetics/genomics, and population science domains involving etiology, environmental and host risk, and cancer prevention.

The successful candidate will enter a vibrant and dynamic research environment with opportunities to collaborate with basic and clinical researchers across diverse disciplines. The Prostate Cancer Program is one of 8 designated research programs in the Fred Hutch/University of Washington Cancer Consortium and is anchored by the NCI Pacific Northwest Prostate Cancer Specialized Program of Research Excellence (SPORE).

Opportunities exist for joint and/or affiliate appointment in the Fred Hutch Divisions of Human Biology, Clinical Research, Basic Sciences, Public Health Sciences, or Vaccine and Infectious Disease, as well as Departments at the University of Washington, depending on mutual interests. Applicants will also be eligible for membership in the Fred Hutch-based Seattle Translational Tumor Research (STTR) program, a multidisciplinary consortium of more than 500 faculty from Fred Hutch, the University of Washington, and Seattle Children’s, who work collaboratively on all aspects of solid tumor basic, translational, and clinical research.

Additional information about Fred Hutch and the Scientific Divisions can be found at: http://www.fhcrc.org/science/

For consideration, applicants need to have a PhD, MD/PhD, or MD or other doctorate degree.

At Fred Hutch, we believe that the innovation, collaboration, and rigor that result from diversity and inclusion are critical to our mission of eliminating cancer and related diseases. We seek faculty members who bring new ways of seeing the world and solving problems. Fred Hutch is committed to ensuring that all candidates hired for faculty appointments share our commitment to diversity and inclusion.

Interested candidates should submit a curriculum vitae; a concise research statement that describes accomplishment and future goals; a diversity statement [describing your past contributions to diversity, equity, and inclusion and your future plans for continuing these efforts as a faculty member (one page or less) and mentoring statement; and the names and contact information of at least three (3) references.

Applications should be received by November 1, 2019 to assure consideration. Applications that arrive after that date may be considered as long as the position remains open.

Overview The Translational Data Science Integrated Research Center (TDS IRC) of the Fred Hutchinson Cancer Research Center invites applications for a faculty position at the rank of Assistant or Associate Member (equivalent to Assistant or Associate Professor). We seek candidates with biological or clinical research programs that develop and use novel computational methodologies, including algorithms or genome-scale biotechnologies, or that use multiple existing techniques together in innovative ways. We especially encourage applications from candidates whose research is related to one of the following: immuno-oncology, single-cell analysis, spatial transcriptomics, machine learning, or cancer genomics. Faculty rank will depend on qualifications and experience.

The Fred Hutchinson Cancer Research Center is a world-renowned research institution with a wide diversity of faculty research programs, spanning fundamental biological research, clinical disease-focused research, and population sciences. The Center has five Scientific Divisions:

* Basic Sciences, focused on fundamental biological research

* Human Biology, which blends fundamental, applied, and translational research performed in model organisms and in vitro systems

* Clinical Research Division, where researchers are continually developing new therapeutic approaches and leading clinical trials

* Vaccine and Infectious Diseases Division, focused on prevention and treatment of infectious diseases

* Public Health Sciences, where researchers apply statistical, behavioral, epidemiological, computational, and translational methods to reduce the incidence and mortality from cancer and other diseases

Fred Hutch faculty and administration are highly collegial, and strongly supportive of junior faculty.

The Translational Data Science Integrated Research Center (TDS IRC), which launched in November 2018, is a cross-divisional, collaborative research effort that will enable the Hutch to leverage recent advances — and spur future innovation — in large-scale biological experiments, computational methods and infrastructure. The TDS IRC promotes collaborative approaches to data science research across all five Scientific Divisions. Faculty rank will be dependent on qualifications and experience.

Qualifications

Applicants should have a PhD or MD. While we particularly encourage candidates with strong quantitative training (e.g., computer science, statistics, bioinformatics or related quantitative disciplines) to apply, candidates without these specific credentials, but who have significant interest in computational science and/or interest in developing new high throughput technologies (as proven by publications and/or grants), will also be considered. The candidate will receive an appointment in the Fred Hutch Scientific Division that is best suited to support the candidate's research program. Fred Hutch has state of the art research facilities, extensive Shared Resources (more information here) and excellent support for scientific computing.

At Fred Hutch, we believe that the innovation, collaboration, and rigor that result from diversity and inclusion are critical to our mission of eliminating cancer and related diseases. We seek faculty members who bring new ways of seeing the world and solving problems. Fred Hutch is committed to ensuring that all candidates hired for faculty appointments share our commitment to diversity and inclusion.

Candidates should send a C.V., a concise statement of research plans and career goal and a diversity statement [describing your past contributions to diversity, equity, and inclusion and your future plans for continuing these efforts as a faculty member (one page or less).

Applications will be reviewed immediately and those received by December 1, 2019 will be guaranteed full consideration for the position. Applications that arrive after that date will be considered as long as the position remains open.

The Fred Hutchinson Cancer Research Center (Fred Hutch) and the University of Washington (UW) are jointly recruiting a full-time laboratory-based faculty member at the Assistant/Associate Member, and Assistant/Associate Professor level WOT (without tenure due to funding), on the Physician/Scientist pathway in the Clinical Research Division of Fred Hutch and the Division of Pediatric Hematology/Oncology, Department of Pediatrics at the UW. The Fred Hutchinson Cancer Research Center, home of three Nobel laureates, is an independent, nonprofit research institution dedicated to the development and advancement of biomedical research to eliminate cancer and other potentially fatal diseases. Recognized internationally for its pioneering work in bone marrow transplantation and immunotherapy, Fred Hutch and the UW provide a unique environment for conducting translational research and clinical care. Fred Hutch in collaboration with its clinical and research partners, the University of Washington and Seattle Children's, is a National Cancer Institute-designated comprehensive cancer center.

The goal is to recruit a prominent scientist/thought leader and translational researcher in the field of pediatric malignancy, with solid malignancies a priority. The successful candidate has an MD, MD/PhD, or PhD, ad is expected to engage in active laboratory and clinical research related to the molecular pathogenesis, genomics/epigenomics, intracellular signaling pathways, or targeted translational therapeutics of neoplasms common in children. Physician faculty member would also participate in the care of patients with pediatric malignancies either in oncology or stem cell transplant service. Candidates must demonstrate a track-record of high-quality peer-reviewed publications, as well as independent research funding or competitive funding potential.

The primary appointment will be in the Clinical Research Division of Fred Hutch. Applicants must have an MD, MD/PhD, or PhD degree (or foreign equivalent) and US Board certification in Pediatric Hematology/Oncology (for physician candidates). Physician candidates, in order to be eligible for sponsorship for an H-1B visa, graduates of foreign (non-U.S.) medical schools must show successful completion of all three steps of the U.S. Medical Licensing Exam (USMLE), or equivalent as determined by the Secretary of Health and Human Services. Fred Hutch and University of Washington faculty engage in teaching, research and service.

Interested candidates should submit a curriculum vitae, and a letter summarizing research goals and career plans to Dr. Soheil Meshinchi at smeshinc@fredhutch.org.

The Fred Hutchinson Cancer Research Center and the University of Washington are affirmative action, equal opportunity employers. Both institutions are dedicated to building culturally diverse faculties and strongly encourage applications from women, minorities, individuals with disabilities and protected veterans.

The Fred Hutchinson Cancer Research Center (FHCRC) is recruiting a full-time faculty member at the Assistant, Associate or Full Member (equivalent to Assistant, Associate, or Full Professor) level to join the Immunotherapy Integrated Research Center ( IIRC) and an appropriate FHCRC Division. The successful candidate for this position will be a prominent thought leader in the field of Cancer Immunology who is engaged in innovative laboratory-based research investigating the regulation of immune responses in the tumor microenvironment, which may include immune checkpoints, stromal interactions, regulatory T cells, myeloid suppressor cells, or other factors that impact tumor progression or regression. This position will be a full-time, multi-year appointment. Candidates must demonstrate an outstanding track record of high quality, peer-reviewed publications of original research in the cancer immunology field, and success in obtaining extramural funding.

The primary appointment will be in an appropriate Division of the FHCRC with a joint appointment proposed at a commensurate rank at the University of Washington (UW). The successful candidate will enter a dynamic research environment with opportunities to collaborate with scientists across a diverse range of disciplines. The Fred Hutchinson Cancer Research Center, home of three Nobel laureates, is an independent, nonprofit research institution dedicated to the development and advancement of biomedical research to eliminate cancer and other potentially fatal diseases. Recognized internationally for its pioneering work in bone-marrow transplantation and immunotherapy, Fred Hutch and the UW provide a unique environment for conducting translational research and clinical care. The Fred Hutchinson Cancer Research Center, in collaboration with its clinical and research partners, the University of Washington and Seattle Children’s, represents the only National Cancer Institute-designated comprehensive cancer center in the Pacific Northwest.

Applicants must have an MD or PhD degree (or foreign equivalent). FHCRC faculty engage in teaching, research and service.

At Fred Hutch, we believe that the innovation, collaboration, and rigor that result from diversity and inclusion are critical to our mission of eliminating cancer and related diseases. We seek faculty members who bring new ways of seeing the world and solving problems. Fred Hutch is committed to ensuring that all candidates hired for faculty appointments share our commitment to diversity and inclusion.

Candidates should send a C.V., a concise statement of research plans and career goal and a diversity statement [describing your past contributions to diversity, equity, and inclusion and your future plans for continuing these efforts as a faculty member (one page or less).

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

Responsible for overseeing strategic and programmatic development across all sites of the SCCA Community Oncology Program to ensure patients receive the most effective, efficient, safest and highest value service across all sites of SCCA care and that community sites are to achieve performance on expected growth, patient access, financial stewardship and program development. The Associate Director of Community Oncology Service Line collaborates with community oncology leadership (Director of Clinical Operations, Director of Business Operations, Assistant Medical Director), analytics, quality, disease team service lines and leaders at SCCA community partner sites to align and achieve these objectives.

Responsibilities

People

• Develops and maintains a culture that fosters an inclusive workplace

Service

• Monitor market conditions and trends that impact the practice of community oncology and of community-academic oncology partnerships. These trends include scientific breakthroughs, technological and other innovations and regulatory changes.
• Lead the development and execution of strategic planning for the community oncology program that supports the overall mission and priorities of SCCA.
• Gain deep understanding of the current state and capabilities of the community oncology program and local, regional and national competitors.
• Gain deep understanding of practice standards, resource needs and productivity output for the community sites.
• Identify critical gaps or new innovative offerings to assure that the care and services offered position the community oncology program for success.
• Develop growth initiatives, access proposals and programmatic improvement efforts across the community sites.
• Analyze, interpret, display, and communicate performance metrics to administrative and clinician leaders particularly in the areas of growth, access, and operational activity volumes.
• Works closely with Outreach and Marketing teams to implement and monitor key components of the referral process and referring provider relationships.
• Responsible for communicating clearly and regularly with SCCA community leadership, community physicians, disease service line leadership and community site leadership and physicians to create alignment across sites and disease programs for programmatic development and access. 

Financial

• Understands the community oncology operational budget
• Exercises fiscal responsibility in decision making 

Qualifications

Required

• Bachelor's Degree
• Experience in health care leadership role
• Emotional intelligence
• Basic understanding of budgets, business planning and work unit operations
• Ability to understand data and how best to use it to establish baseline/current state and make decisions to affect change.
• Critical Thinking – ability to synthesize a large amount of information, anticipate needs and draw accurate conclusions.
• Problem Solving – ability to grasp details of a situation quickly and convert thinking from listening & learning to volunteering and facilitating solutions.
• Systems Thinking – ability to understand interdependencies and how decisions impact complex systems
• Ability to communicate verbally in person, on the phone, in writing or through other visual forms in a clear concise and professional manner
• Presentation skills that effectively convey complex information in a way that engages administrative and clinical leaders and provides a basis for understanding and decision-making.
• Ability to facilitate diverse groups to achieve common understanding, consensus and decision-making.
• Ability to work vertically and horizontally with people of various educational, professional, and organizational differences.
• Proficiency in Microsoft Word, Excel, and PowerPoint

Preferred

• Master's Degree in Health Administration, Business, or related field
• Oncology experience
• Experience with process improvement methodologies
• Minimum of 7 years of progressive leadership experience in an academic or community health care setting including experience leading teams, onboarding new sites of practice and integrating patient care across multiple organizations.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Statistical Center for HIV/AIDS Research and Prevention (SCHARP) at Fred Hutch is a full service statistical and data management center focused on HIV prevention research. SCHARP has an annual budget of over $40 million, more than 180 employees and is currently managing over 40 active phase I – III clinical trials in over 150 clinical sites around the world. SCHARP is seeking an Associate Director, Clinical Data Management (CDM) to provide overall leadership and management of the clinical data management and safety teams (consisting of 40 staff) and direct supervision of CDM managers, the manager of Clinical Safety and Coding, and other CDM staff as needed. The incumbent will be responsible for ensuring that the CDM teams are operating efficiently and effectively and that they meet the requirements of the research protocols in a regulatory compliant manner.

Responsibilities

Leadership  

• Provide overall strategic, organizational, and operational management and guidance to the Clinical Data Management group. 
• Collaborate with the SCHARP Director and other senior managers to create and implement overall organizational vision and strategic direction. 
• Foster and promote the long-term development of the Clinical Data Management team, work closely with the SCHARP Director, Senior Management Team, and the CDM managers to improve the operational effectiveness of the group.

Management 

• Directly supervise Clinical Data Management and Safety and Coding managers, and other CDM staff as needed. 
• Provide training, direction and performance management for individual employees and work with Fred Hutch Human Resources staff to facilitate recruiting efforts and staffing changes as needed. 
• Develop and maintain CDM staff morale, engagement, and professional development. 
• Monitor group project and protocol workflows, priorities, timelines, deliverables, documentation and resources and communicate issues regarding conflicts and/or resource limitations. 
• Provide technical and functional oversight of the day-to-day work and work products of clinical data management staff, as needed, including clinical data collection, processing, and quality control procedures, timelines and documentation.

Change Management and Quality Assurance 

• Lead departmental efforts to standardize work practices and develop standard operating procedures in conformance with GCP, GCDMP, and ICH guidelines, and that meet regulatory submission requirements, and CDISC standards. 
• Oversee and ensure quality assurance of CDM in coordination with the Quality Management section. 
• Prioritize and manage the implementation of SCHARP continuous quality improvement, regulatory compliance, operational effectiveness, and technical infrastructure improvement projects in clinical data management. 
• Evaluate and identify efficiencies and process improvements including leading process improvement projects, and infrastructure and technological upgrades to improve CDM intake, workflow, documentation, tracking, and protocol management 

Qualifications

Minimum: 

• Bachelor’s degree in related field and a minimum of 10 years of experience in clinical research, data management or related field, of which 4 years is in a leadership or management role, or equivalent combined years of education and experience.
• Demonstrated leadership, management, supervisory, and collaboration skills across functions to drive effective and efficient Clinical Data Management practices. 
• Excellent project management and organizational leadership and change management experience. 
• Experience in the development and use of commercial clinical data management. Systems and/or EDC products. 
• Advanced knowledge of clinical research, FDA, ICH, GCP, GCDMP, and related regulatory requirements and best practices.

Preferred: 

• Graduate Degree in life sciences or related disciplines. 
• 10+ years management experience in a clinical research organization. 
• Organization strategic planning experience. 
• Working knowledge of CDISC / CDASH, MedDRA coding, and Medidata Rave EDC. 

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Associate Vice President is a key member of the Office of Research Administration and Faculty Affairs, partnering with and supporting the Vice President for Research Administration and Faculty Affairs in the optimization of critical administrative infrastructure that supports world class research and scientific innovation at Fred Hutch. 

The Associate Vice President will provide leadership and oversight to key functions within the Office of Research Administration and Faculty Affairs and serve as a research administration business process expert for collaborative, cross-functional initiatives and projects, process re-engineering and application implementations, and execution of vision and strategy.  This role works in partnership with administrative, scientific division, shared resources, process improvement, internal audit, and strategy offices, as well as Center executive leadership. 

The Associate Vice President will be a trusted partner of the Vice President in all areas of the Office’s activities and a key point of contact and support for the scientific divisions and faculty.  The incumbent will have a deep understanding of scientific research and research support services, with strong subject matter expertise in one or more research administrative or compliance areas.  The successful candidate will have demonstrated management experience, strong interpersonal skills, and a reputation for being collegial, diplomatic, and respectful.  Together with the Vice President, the incumbent will promote a culture of community, inclusivity, competence, accountability, and innovation among the Office’s units.

Responsibilities

• In collaboration with the Vice President, develop and articulate short-term and long-term strategic plans and initiatives.
• Oversee the daily operations of the Conflict of Interest Office and provide direct management of the RAFA Project Manager and other staff, as assigned.
• Lead workforce development initiatives in support of the community of research administrators across the divisions and central administration, in partnership with Senior Operations Directors of the 5 scientific divisions and Human Resources.
• Coordinate the annual budget request and review cycle.
• Develop, manage, and execute special projects and initiatives related to enhancing research support services.
• Develop metrics and dashboards to measure and display the successes and ROI of the office.
• Prepare and disseminate reports, annual summaries, and presentations to Center stakeholders, as directed by the Vice President.
• Manage and coordinate major communications about key Research Administrative and Faculty Affairs initiatives with internal partners and stakeholders, as directed by the Vice President.
• Coordinate the development and implementation of policies, procedures, and templates to support the successful career advancement of Fred Hutch faculty.
• Represent the Office of Research Administration and Faculty Affairs as an expert in collaborative, cross-functional initiatives and projects, process re-engineering and application implementations.
• Other duties as assigned by the Vice President.

Qualifications

• Master’s Degree or equivalent required. PhD strongly preferred.  
• Minimum 10 years demonstrated achievement in research and staff management in a complex organization.
• Demonstrated ability to initiate, develop, and implement new programs, processes, and initiatives.
• Broad knowledge of research-related policies and regulations., including FDA, human and animal research protections, federal grants policy, and conflict of interest. Expertise in one or more research- or compliance-related areas.
• Excellent interpersonal, oral, and written communication skills.
• Must be highly detail-oriented and organized with intermediate knowledge of Microsoft Word, Excel, Outlook, PowerPoint, and SharePoint.
• Demonstrated capacity to manage highly sensitive and strictly confidential material.
• Ability to solve complicated, sensitive, confidential issues quickly in a fast-paced environment.
• Self-starter, able to work under minimal supervision.
• Thorough understanding of the goals and mission of Fred Hutch.

The Fred Hutchinson Cancer Research Center invites applications from scientists working in the area of breast cancer research to lead a translational research program. Applicants will be considered at the rank of Associate or Full Faculty member, and we are seeking individuals who share our goals to advance an understanding of the biological basis of breast cancer, and to translate findings to the clinic.

We will consider PhD, MD/PhD, or MD scientists working in areas that include, but are not limited to: steroid receptors, signaling pathways, microenvironment, metastasis, systems biology, computational biology, and the biology of therapeutic response/resistance, genetics/genomics. A track record of relevant publication and funding commensurate with appointment level is highly desirable. Physician-scientists in any relevant medical discipline are encouraged to apply.

The successful candidate will enter a vibrant and dynamic research environment with opportunities to collaborate with basic and clinical researchers across diverse disciplines. The Breast and Ovary Cancer Program is one of 8 designated research programs in the Fred Hutch/University of Washington Cancer Consortium.

Opportunities exist for joint and/or affiliate appointment in the Fred Hutch Divisions of Human Biology, Clinical Research, Basic Sciences, Public Health Sciences, or Vaccine and Infectious Disease, as well as the University of Washington, depending on mutual interests. Applicants will also be eligible for membership in the Fred Hutch-based Seattle Translational Tumor Research (STTR) program, a multidisciplinary consortium of more than 500 faculty from Fred Hutch, the University of Washington, and Seattle Children’s, who work collaboratively on all aspects of solid tumor basic, translational, and clinical research.

Additional information about Fred Hutch and the Scientific Divisions can be found at:

http://www.fhcrc.org/science/

Overview

Seattle Cancer Care Alliance (SCCA) brings together the leading research teams and cancer specialists of Fred Hutch, Seattle Children’s, and UW Medicine. One extraordinary group whose sole mission is the pursuit of better, longer, richer lives for our patients. SCCA's purpose is to provide state-of-the-art, patient and family centered care; support the conduct of cancer clinical research and education; enhance access to improved cancer interventions; and advance the standard of cancer care regionally and beyond.

Every individual at SCCA plays a unique role in supporting our mission. Our collective success hinges on each of us conducting ourselves in accord with a set of core values:

• We are patient-centered. Everything we do must be linked to our ability to deliver better, safer outcomes for our patients.
• We are innovative. We nurture an environment that fosters unconventional thinking, a passion for discovery, and the open-mindedness to invite discovery from unexpected places.
• We are respectful. We are deeply respectful of our patients, their families, and each of our colleagues who serve them in so many different and important ways.
• We are collaborative. We understand that asking for and offering help in how to do better is not just a right, but among our most important responsibilities.
• We are agile. We cannot just be comfortable with change; we must embrace it as proof that we are making progress.
• We are responsible:  Because our work is focused on people's well-being, we approach it with the highest level of ethical, fiduciary, and environmental responsibility.

The Learning Management System Domain Administrator (DA) has an active role in the day-to-day management of the LMS application.  Within their domain, they are responsible for the management of onboarding of business units, the maintenance of the business units, eLearning, and the maintenance of the LMS. This person maintains the SCCA Learning Management System. This position will also manage eLearning projects to meet organizational and regulatory needs as well as support enterprise projects.

Responsibilities

• Collaborate with business units and stakeholders in domain to identify and incorporate all learning, enrollment, and reporting requirements into the LMS using consistent standards.
• Collaborate with instructional developers and trainer to ensure training content meets LMS and SCORM requirements
• Develop and maintain LMS system standards, policies, procedures and related documentation for domain.
• Onboard new business units to determine business requirements and extent of training needs.  This includes analyzing structures, onboarding Super Users, reports and training
• Develop and monitor project plans and ensure scope is maintained
• Participate in the testing of system upgrades and functionality changes
• Work closely with SME to create eLearning which includes creating, testing, determining activity requirements and launching of content
• Strong customer service skills to support internal and external customers

Qualifications

• Bachelor’s degree in Computer Science, Communications, Instructional Design or a similar field or four years application support experience 
• 2 years of demonstrated experience working with Learning Management Systems
• Demonstrated skill in administering and supporting eLearning systems with internal and external customers.
• Demonstrated experience developing eLearning modules.
• Expertise in customizing web pages, modifying web parts in an LMS / content management system / portal / SharePoint, or other collaborative platform.
• Proficiency in all Microsoft Office applications. 
• Must have strong organizational and project management skills. 
• Ability to use initiative and sound judgment in carrying out responsibilities
• Ability to organize time effectively, determines priorities, and move work forward independently.
• Excellent interpersonal skills with the ability to work and communicate with all levels of the organization. 
• Exhibits excellent teamwork and ability to collaborate with cross functional team members

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

Reporting to the Director of Total Rewards, the Benefits Manager is responsible for the planning, design, implementation, and administration of an overall benefits and wellness strategy to ensure market competitiveness, fair internal practices and alignment with the organization’s mission, vision and values. This includes creatively maximizing internal awareness and utilization of our programs, building efficiency, and managing costs. The Manager also leads the end-to-end leave of absence program, including program design and administration with a focus on the employee experience, policy and legal compliance and continuous improvement.

Responsibilities

• Drive service delivery, administration, participant communication/education, cost management and compliance processes for employer-sponsored employee benefits, wellness and leave of absence programs.
• Responsible for the strategic vision and cultural alignment of the Wellness Program, as well as achievement of that vision through various wellness initiatives and goals.
• Manage the administration of Leave of Absence programs/benefits; drive timely notification, documentation, eligibility review, and benefit coordination.
• In partnership with the Director of Total Rewards, oversees the planning and administration of all activities related to annual benefit renewal process and open enrollment.
• Research and resolve benefit issues to ensure a positive employee experience while maintaining confidentiality at all times.
• Deliver consistent, effective, and accurate communication with program participants; produce presentations and program materials including required notices and program-related updates.
• Evaluates, designs and recommends program offerings and modifications based on overall effectiveness, benchmarks, market assessment, business strategy and cost impact.
• Lead, develop and manage benefits team members, emphasizing service delivery, accountability and continuous improvement.
• Conduct regular audits and reviews of processes, documents, tools, and workflows to ensure data quality, process effectiveness, and compliance with program and regulatory requirements.
• Leads mapping of benefits and wellness processes and programs and ensures documentation of all programs and process with a focus on consistency and creating the ability to scale.
• Responsible for due diligence and successful integration, related to mergers and acquisitions for benefits.
• Manage internal reporting of plan metrics, including monitoring of the self-funded claims experience, and benefit plan expenditures to identify trends and make recommendations to minimize plan and budget risks.
• Manages vendor relationships including benefits consultants, brokers, third party administrators and other external service providers by building strong relationships and overseeing vendor performance.
• Reviews and analyzes changes to state and federal laws related to benefits and reports/recommends changes to management.
• In concert with Director, present detailed and comprehensive benefits recommendations to internal senior stakeholder/leaders and the board.
• Develops and communicates a compelling vision for wellness that motivates and engages employees to increase healthy behaviors for the long term.
• Ensures that development and implementation of benefits programs, policies and practices are in compliance with ERISA, COBRA, FMLA, HIPAA, ACA, ADA, Seattle Sick-Safe, WA Paid Family Leave and other applicable federal, state and local laws and regulations.
• Maintains and implements schedule of governmental benefit filings (Form 5500, etc.)
• Formally educates employees and supervisors/leaders on Leave Management.
• Interpret and advise HR team on benefit changes; provide training and guidance as required.
• Lead third-party relationships for global benefits programs including consultants/brokers and carriers.
• Anticipate legal changes for leave requirements across the U.S. and proactively identify solutions to ensure compliance and employee experience.
• Serve as primary support for sensitive and escalated employee concerns, appeals and claims.
• Identify process improvements to provide an enhanced employee experience.
• Work across multiple departments to ensure information is consistent, engaging and available.
• Other duties as assigned.

Qualifications

Required:

• Bachelor's degree in business management, human resource management or other related field, and/or commensurate experience in benefits management.
• 5+ years’ directly-related full-cycle benefits experience in a Human Resources department setting.
• 3+ years’ supervisory experience.
• Must have experience administering multiple plan renewal and open enrollment cycles.
• In-depth understanding of features and mechanics of a broad variety of employee benefit and retirement programs.
• Solid understanding of ERISA and all applicable requirements, regulations, and federal and multi-state laws relating to employee benefit programs, qualified retirement plans and leaves of absence.
• Demonstrated success implementing and sustaining effective Wellness program including the measurement of impact/effectiveness.
• Knowledge of best practices and processing requirements relating to leave management.
• Ability to effectively articulate benefit plan options to a wide range of audiences.
• Demonstrated ability to drive complex projects to completion using effective project management, communication and influence skills.
• Experience interpreting and communicating policy requirements.
• Ability to critically analyze problems and develop solutions.
• Excellent verbal and written communication, collaboration and customer service skills.
• Strong attention to detail and ability to work under daily deadlines while handling multiple tasks.
• MS Office proficiency.

Preferred:

• Experience in the administration of benefits programs in a multiemployer/union plan environment is highly preferred.
• Experience with administration of benefits programs in multiple states preferred.
• Workday experience preferred.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here

A Computational Biologist/Bioinformatics Analyst position in the laboratory of Dr. Gavin Ha and the Computational Biology Program is available immediately. We are seeking a highly motivated individual who is interested in studying the genetics and epigenetics of cancer using computational approaches. Candidates who are excited about large/complex ‘omics’ data analysis and cancer research are encouraged to apply. 

Responsibilities

The Ha lab is establishing a research program that uses new DNA sequencing technologies to study cancer genomes. The lab is also focused on research involving liquid biopsies, such as cell-free DNA, and developing new computational approaches to leverage these data for genome discovery and cancer burden monitoring. The research interests/projects in the Ha lab include:

• Analysis of cancer genomes to understand tumor progression/evolution, metastatic disease, non-coding genome alterations, copy number alterations, genome rearrangements and 3D structure, mutational signatures
• Development of novel computational algorithms for long-range (linked-reads or long-reads) whole genome sequencing of tumors
• Development and analysis of sensitive approaches to detect tumor-derived DNA in cell-free DNA from patient blood plasma
• Analysis of tumor microenvironment and heterogeneity using single-cell RNA sequencing
• The lab works with collaborators to validate results using functional experiments
• For examples of recent studies, see PMID:29909985, PMID:29109393, PMID:25060187

Candidates with strong interest and/or expertise in any of these research areas are highly encouraged to apply

• Cancer genomics, liquid biopsies, tumor evolution/heterogeneity, single-cell transcriptomics
• Application of statistical modeling, algorithm design, artificial intelligence to study cancer and genetics
• Analysis of large, complex genome, epigenome or transcriptome data

Qualifications

Applicants must have at least a Bachelor’s degree in one of these disciplines:

• Computational biology, bioinformatics, computer science, data science, statistics, biostatistics, biomedical engineering, computer/electrical engineering, physics, biochemistry, or other related fields

Applicants should have some of the following skills and experience:

• Work well in team environments; strong communication skills; detail-oriented
• Strong programming experience (R, Python, Matlab, Java, C/C++, Perl or other languages for research)
• Experience with high performance computing environments or cloud computing environments is a plus
• Experience with analyzing sequencing data is considered a strong asset
• A background in cancer biology is considered a strong asset.

Submission of a targeted cover letter is strongly recommended.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The successful candidate will work with a diverse group of technical staff and bioinformatics specialists to support the wide ranging genomics data analysis needs of Fred Hutch faculty and staff. The Bioinformatics Analyst will report to the Bioinformatics Shared Resource Manager, in association with the Director of the Genomics and Bioinformatics Shared Resources, and will work with Fred Hutch scientists to refine computational research questions and develop analytical processes that can be applied to genomics datasets.

Responsibilities

Job Duties:

• Work closely with Genomics staff to bring new instrumentation online, implement new analysis workflows, and maintain laboratory operations including automation of routine data processing and routing to end-users.
• Develop, implement, and test standardized analytical pipelines to support common NextGen sequencing assays (e.g., RNAseq, ChIPseq, SNV/CNV).
• Communicate with researchers and identify appropriate bioinformatics tools to meet the needs of proposed research projects.
• Provide support to Fred Hutch statisticians, bioinformaticians, and computational biologists working with genomics data.
• Participate in weekly staff meeting to discuss ongoing projects and provide advice and support to colleagues.
  Provide figures & written sections describing methods and results for manuscripts, presentations, and grant applications generated by Fred Hutch researchers.

Qualifications

Individual will have a bachelor's, master's or PhD degree in computer science, bioinformatics, biology, genetics, or related discipline with significant computational emphasis and at least 3 years of relevant experience working with genomics data. The individual must be proficient with Linux/Unix shell scripting (primarily bash) and possess strong programming skills in Python and R. Knowledge of Java or C++ a plus.  Must have a proven track record of deep sequencing analysis showing a working knowledge of standard analysis tools (e.g., GATK variant calling pipelines, alignment & pseudoalignment based RNA-seq quantitation, Bioconductor packages) and relevant databases. The individual should be self-motivated, perform in a highly independent manner, and possess strong interest in the biological sciences.  Solid communication skills (both verbal and written) and organizational skills are essential, as is the ability to be creative in problem-solving situations.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer with minimal side effects. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first and largest cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Uganda Cancer Institute/Hutchinson Center Cancer Alliance (“UCI/HCCA”) is a collaborative undertaking that has established a state-of-the-art cancer treatment and research facility located in Kampala, Uganda. The activities carried out by the Hutchinson Center in Uganda in support of this alliance are performed under the auspices of the Hutchinson Centre Research Institute of Uganda (“HCRI-Uganda” or “HCRI-Ug”). A primary objective of the collaboration between the Global Oncology Program at the Hutchinson Center and the Uganda Cancer Institute is the development of innovative, low-cost cancer prevention and treatment strategies that are appropriate for low- and middle-income countries (LMICs). The UCI/HCCA also has a strong focus on ameliorating the high burden of infection-related cancers in LMICs. Clinicians and scientists at the UCI/HCCA work together to enhance patient access to care, diagnosis, and research-based treatment. In addition to the UCI/HCCA, the Hutchinson Center’s Global Oncology Program supports research activities in several other countries, which collectively carry out the mission of the Program to conduct high-quality research and capacity-building on an international scale.

This individual will serve as a Biorepository Technician for the Global Oncology Program’s laboratory operations which operates at the UCI – Fred Hutch Cancer Centre (“UCI – FHCC”), a 25,000-square foot cancer research and treatment building on Mulago Hill in Kampala that opened in May 2015. The laboratory facilities of the UCI – FHCC are primarily located on the third floor of the building and include a Specimen Processing Lab, Molecular Diagnostics Lab, Histopathology Lab and BSL2+ Lab. There is also dedicated space on the third floor for a future Immunology Lab.

The Employee will serve and train under the immediate supervision of the Laboratory Director and will be based in Seattle full-time.  The incumbent will report to the Laboratory Director. The incumbent’s primary responsibility will be to manage and ensure the proper functioning of all daily activities within the Global Oncology’s biorepository on the Seattle side and work cohesively with the Laboratory Data Coordinator in Kampala for the HCRI-Ug. Additionally, they are expected to organize, receive and QC/QA all shipments for samples and reagents going between the two sites under the supervision of the Laboratory Director. The Biorepository Technician will act as a liaison between the Laboratory Director and the study teams, the Fred Hutch research cell bank and Freezer Farm along with collaborators in regard to responsibility for all samples that are accrued and banked with the Global Oncology Program. The position will require the individual to be knowledgeable in all laboratory activities as well as other project activities that pertain to the laboratory and its scientific development and GCLP and biobanking.  The individual may be required to assist the Laboratory Director in teaching new technicians, visiting scientists and students in laboratory practices pertaining to the repository.

In addition to the Global Oncology Program, the Biorepository Technician will spend at least 40 percent of their time with the Warren Laboratory in the Immunology Department which is a part of the Clinical Research Division.  This role will be similar to assisting with the Warren Laboratory’s biorepository, shipping and receiving and act as a liaison between the Warren Laboratory and the UW study teams, the Fred Hutch research cell bank and Freezer Farm along with collaborators in regard to responsibility for all samples that are accrued and banked with the laboratory’s ongoing studies.

Responsibilities

1. Applicants demonstrates and promotes Good Clinical Laboratory Principles (GCLP) in all areas of responsibility.
2. Operate independently to resolve issues as they arise, utilize good judgment to determine if additional resources, staff or supervisor needs to be notified or included in decision making.
3. Communicate with multiple internal and external working groups, investigators and organizations to ensure repository shipping requirements and obligations are met with high customer service standards. 
4. Perform specimen processing laboratory back up activities including; the isolation and cryopreservation of Peripheral Blood Mononuclear Cells (PBMC) from whole blood or leukapheresis, serum, plasma and semen isolation and freezing and understanding of HIV clinical trials protocol logistics and specimen requirements.
5. Help support in conjunction with the Laboratory Director to oversee and train new lab staff and students in repository safety, operations, procedures and handling of hazardous materials.
6. Demonstrate working knowledge with Laboratory Information Management Systems (LIMS) and Microsoft Access, including queries, form building and reporting.
7. Develop/update, create and maintain SOPs and other guidance and reference materials relevant to specimen handling /shipping and their logging into the inventory database related to their respective repositories.
8. Function as primary repository floor liaison and responder with Fred Hutch facility engineers and external vendors on repository projects including planning, logistics, technical equipment inquiries, alarms, supplies and other various tasks related to the startup operations and maintenance of expanded repository space and functions.
9. Function as liaison with LIMS programmers to develop and define user requirements, functionality, work flow, inquiries, data migration, data transfer and reporting features for new Labware LIMS systems. Report on progress, anticipated or existing problems, and discuss the work to be performed with the repository manager, lab manager and LIMS programmers.
10. Perform and document quality control procedures and maintain accurate records for cleaning, maintenance and monitoring activities for temperature sensitive equipment, specimen management, shipping and receiving for domestic and International biological research specimens and reagents according to IATA requirements.
11. Draft and review SOPs, SSPs, Lab Manuals and Study Plans where needed pertaining to biobanking and the biorepository primarily in Seattle.
12. Familiarize with the GO Laboratory SharePoint Site and the HCRI-Uganda Laboratory Server
13. Establish and maintain a good relationship with the other laboratory sections in the UCI-FHCC (pharmacy and STAT clinic lab) and support those sections in biorepository and sample maintenance, training and documentation.
14. Oversee the coordination of other vendor/collaborator contract/agreements and renewals (g., standing orders, annual quotes from major suppliers, etc.) for reagents, consumables, PPE, and other laboratory supplies. Manage the HCRI-Uganda Ordering List.
15. Help support when needed all laboratory supply and ordering needs in coordination with the Procurement Officer, Laboratory Director and Laboratory Technicians to ensure that at all times supplies are available for use in the Laboratory for the UCI-FHCC team.
16. Familiarize with the FH Financial Management System for ordering of supplies, equipment and services.
17. Together with the Laboratory Director oversee initial and annual competency and proficiency of employees on each research and clinical assay.
18. Assist the Laboratory Director in the set-up of GCLP compliance with the goal of future accreditation or maintaining accreditation, as appropriate, in UCI – FHCC component laboratories.
19. Prepare for and participate in internal/external audits of the laboratory.
20. Oversee maintenance and training on the specimen tracking system Freezerworks.
21. Oversee and perform quarterly audits of GO and Warren Laboratory biorepository specimen storage to assess accuracy and completeness.
22. Oversee pulling of specimen for shipment. Review Shipping paperwork if needed. Supervise local and international shipment of samples. Establish a relationship with local and international shipping courier services.
23. Work closely with the HCRI-Ug Procurement Officer and administration for obtaining URA tax exemptions and National Drug Authority verification letters for shipment. Familiarize with the NDA Portal. Work closely with HCRIU regulatory office for further permits if needed.
24. Ensure that the laboratory maintains a clean and safe working environment. The Laboratory Manager should coordinate these activities with the HCRI-Ug Laboratory Safety Officer and EH&S Officer.
25. Work Occasional off-hours (evenings and weekends) in response to out-of-range freezer alarms or equipment malfunction.
26. Must have a positive attitude and patience and a good work ethic.
27. Other duties as assigned.

Qualifications

A bachelor’s degree in the biological sciences and laboratory bench research experience are required.  Experience with cell culture techniques, and blood processing is preferred.  The technician must show initiative, the willingness to take up new skills and responsibilities, and be a team player. Excellent attention to detail and the ability to work independently are essential to success in this position, as are good communication and organizational skills. Salary will be commensurate with (appropriate) experience.

• IATA biological diagnostics, dangerous goods and infectious substances shipping preferred.
• Bachelor’s degree with 3+ years of experience.
• Extensive knowledge and proficiency in working in a GCLP and clinical trial environment.
• Previous experience in an accredited laboratory is preferred.
• Proficiency in a variety of laboratory assays and techniques and lab operation.
• Experience with oncology or Infectious disease preferred.
• The successful candidate must be able to work accurately and efficiently, be detail oriented, and work both independently and within a group.
• Strong troubleshooting and problem-solving skills are required.
• This position requires excellent written and verbal communication skills and the ability to work positively in a group environment.
• A high degree of professionalism and management ability is required of this position as well as interpersonal abilities to motivate individuals to perform in an efficient and productive manner
• The candidate in this position must be flexible and skilled at organizing and prioritizing tasks. Familiarity with Microsoft Word, Excel, and Internet Explorer is desirable.
• Familiarity with a laboratory information management system (LIMS) such as Freezerworks is a plus.
• Biobank training or IATA dangerous goods certification training is preferred

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The Business Analyst III performs data discovery and uses technical expertise to design, create and develop automated analytic solutions to support budget and financial management reporting. The primary purpose of the role is to support financial decision making of the organization to ensure the short-term and long-term financial success of the SCCA. The position reports to the Associate Director of Financial Planning & Budget.

Responsibilities

• Design and implement automated analytic solutions, including reports, dashboards, and views from a wide range of data sources, and provide leadership in evaluating, interpreting and optimizing these solutions.
• Assure integrity of the data for current and future financial reporting and ensure the sustainability and adaptability of all developed solutions. Seek opportunities for continuous improvement.
• Collaborate interdepartmentally to monitor and develop meaningful reports that provide users with insight on financial performance.
• Develop a robust understanding of SCCA’s financial data and systems to ensure effective, reliable, and responsible use of data.
• Build systematic solutions that address complex business problems, derive actionable insights, and maximize decision-making confidence, while being easy to refresh.
• Utilize numerous data sources and analytics to develop reports that assist in conveying the causes of financial variation. Assist in developing action steps for financial improvement and reports to monitor these results.
• Maintain a solid working knowledge of a wide range of internal financial systems, workflows and related data sources.
• Conduct data discovery and analysis from financial data to generate and test working hypotheses, uncover relationships and identify data quality issues.
• Manage budget system (currently Kaufman Hall Axiom) from a data management and reporting perspective.
• Translate business problems into technical approaches to create standardized Tableau reporting dashboards which help explain budget to actual variances and guide decision making.
• Other duties as assigned

Qualifications

Required:

• Bachelor's degree (BA or BS) required - preferably in Informatics, Math, Business, Computer Science or related field, or equivalent combination of education and experience/technical training that demonstrates analytical and technical competency
• 5 years of business analytic experience, preferably in a healthcare environment or relevant experience
• Superior organizational skills and proven knowledge and application of best practices for system management, documentation and standardization.
• Sustained, proven ability to think systematically and analytically and use independent judgment.
• Ability to identify and implement areas of improvements such as increasing the level of data accuracy or decreasing the time spent to update a model or report.
• Experience with financial software programs such as Kaufman Hall/Axiom, Tableau, PeopleSoft, Workday.
• Advanced Excel skills and experience with relational database tools such as SQL Server and Access.
• Ability to research, analyze and interpret complex data and formulate recommendations.
• Collaborative and team-oriented communication style able to work effectively cross departmentally.
• Excellent verbal and written communication skills, including the ability to propose actions, identify and illustrate opportunities, make recommendations and articulate financial impact of decisions to both clinical and administrative audiences
• Solid financial skills, including a working understanding of the income statement.
• Able to grasp and apply new concepts quickly.
• Ability to effectively prioritize concurrent responsibilities and meet timelines.
• Ability to work independently under minimal supervision with a wide degree of creativity and latitude. May manage projects independently or lead/direct the work of others.
• Ability to work in a high pressure, deadline oriented, and complex health care environment.

Preferred:

• Master’s Degree in Health Science, Informatics, Business or a related field preferred
• Experience in managing databases and systems.
• Extensive experience in exploratory data analysis, data visualization.
• Experience with predictive modeling and leading indicators
• A working understanding of the relationships between the income statement, balance sheet and cash flow statement.

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The main function of the Financial Systems Group is to be the liaison between IT and Financial Operations to including data analysis, documenting business requirements, system troubleshooting, audit support, project re-implementation support and conducting file uploads, query and reporting development and training. The team is comprised of 4 individuals: Financial Systems Manager, Sr Business Analyst, and two Business Analyst III.

Responsibilities

We are seeking a Business Analyst III who has a holistic understanding of PeopleSoft data, table, and integration architectures.  The following outlines but does not limit the role responsibilities:

Primary Support:

• PeopleSoft Asset Management, Project Costing, Cash Management/Treasury, and Supplier Contracts Management
• Support PeopleSoft FMS and interface upgrade efforts and trouble shooting
• Support financial systems patches, updates and implementation efforts to include testing, procedural documentation and data mapping/migration
• Troubleshoot PeopleSoft systems to ensure accurate transactions
• Develop system process, procedure, testing and training materials
• Support CPI process improvements

Secondary Support:

• PeopleSoft AP, AR, Billing (other PeopleSoft modules, as able), plus Tableau Reporting.
• Epic system posting and reconciliations to the general ledger
• Support Epic audit activities to include developing schedules, reconciliations and coordination with process owners and related documentation/justifications
• Develop Epic Revenue and AR (Cognos and BOE) report specifications, complete testing and research transaction abnormalities
• Conduct payroll troubleshooting and system improvements to eliminate manual entries
• Conduct PeopleSoft file uploads to include Payroll, Epic and budget transactions

Qualifications

Required:

• Bachelor’s degree
• Two years of experience in accounting or finance to include project costing and revenue reconciliation
• Proficient with MS Office tools (Excel, Word, Visio)
• Good analysis and problem solving skills
• Excellent written and verbal communication skills
• Ability to accept direction and multi-task
• Exhibit professional, dependable, reliable, and collaborative work habits

Preferred:

• Proficient with PeopleSoft Financials and Supply Chain version 9.2
• 3-5 years of business requirements development and documentation to include system testing and implementation
• 3-5 years of experience in Healthcare accounting
• Proficient with Cognos and BOE

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Business Operations Analyst performs financial and operational activities to ensure the departments core business processes run smoothly and are well managed and executed. The business operations analyst role is the anchor for the operations of the organization in support of management financial and operational processes. The Business Operations Analyst works independently and is expected to use initiative and sound judgment in carrying out the day to day responsibilities to support of the Hutch Data Commonwealth (HDC).

Key areas of focus include:

• Vendor management (invoice processing, contract assessment and renewals, etc)
• Managing chargeback processes across the organization for centralized services
• Internal operational expense management and reporting
• Project and capital asset depreciation process support
• General billing and accounts management functions

The Business Operations Analyst reports to the Director of Business Operations

Responsibilities

Operational

• Manage end to end process for all for HDC managed licensing and maintenance contracts
• Facilitate process to ensure all invoices are validated, processed and payments made in a timely and accurate manner.
• Partner with department leadership and staff to provide guidance on processes related to vendor engagement
• Coordination with Finance team in billing preparation for external customers.
• Create purchase order requisitions that are within the scope of the business operations
• Collaborate with cross functional teams across the organization to investigate, troubleshoot and resolve budget/financial operational related errors and issues effectively.
• Identify process improvement areas and work across teams to identify solution and deliver improvements.
• Compile, validate and reconcile procard statements and receipts for departmental cardholders.
• Provide ongoing support to the business operations team and other areas of HDC. This includes completing special projects, assignments and administrative tasks as required.

Financial operations

• Prepare journal entries to support internal chargebacks as well as invoice adjustments.
• Prepare ad-hoc financial reporting when requested by department, Finance or Accounting.
• Support month end accounting close and ensure all deliverables are completed by required due dates. Responsibilities include the preparation of accruals, variance analysis and provide information to Accounting and Finance as necessary.
• Assist with the preparation of the annual budget and forecasting
• Manage HDC’s grant allocation
• Provide support to the HDC leadership. This includes completing special projects and assignments as required.

Qualifications

• Bachelor’s degree in business administration/finance or equivalent experience
• Minimum of 3-4 years related to business financial operations. Preferred experience in Research/IT environment
• Strong business acumen in the area of financial operations in a non-profit environment
• Highly proficient with MS Office applications, including Outlook, Word, Excel, SharePoint and PowerPoint.
• Experience with Tableau reporting
• Proven ability and drive to identify and implement process improvements
• Excellent problem-solving, information gathering, and analysis skills
• Natural ability to work in a fast-paced, ambiguous environment
• Highly organized and have a demonstrated ability to plan, prioritize time, and execute on deliverables
• Very detail oriented and work with a high degree of accuracy.   
• Excellent interpersonal skills and professional diplomacy
• Excellent verbal and written communication skills

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Clinical Research Support Director of Clinical Operations is responsible for direct oversight of programs that support start-up, scientific review, and NCI data reporting for Cancer Consortium clinical research. The incumbent leads the relevant operational design and oversight of the Clinical Trial Management System (CTMS). The incumbent defines and report metrics to study teams and Consortium administration working towards system improvements within the incumbent’s team, as well as throughout the Consortium.

The incumbent manages multi-disciplinary teams. They will attract, develop, and retain strong teams; contribute to short and long-term organizational planning and strategy as a member of the management team to strategize growth and resource utilization. The position reports directly to the Director of CRS.

Responsibilities

Oversee central study startup program:

• Manage, oversee, and scale trial startup portfolio to ensure coordinated study reviews, budget and contract negotiations, and compliant source documentation within the Consortium
• Work across CRS teams and other partner organization functions needed to support study startup
• Gather and report study startup metrics and status on a regular basis
• Identify study startup process issues and resource needs across the Consortium; propose and implement solutions
• Create tools to manage the study startup process
• Represent Consortium start-up processes and central support to leadership, faculty, study teams, and external organizations
• Lead efforts to improve start-up processes across the Consortium

Direct the startup protocol review and data reporting functions:

• Oversee committee management for the Scientific Review Committees (SRC); ensure that the Consortium meets NCI’s requirements for the SRC including start-up, trial prioritization and trial accrual rates.
• Propose and manage Consortium policies to ensure the Consortium meets SRC and data reporting requirements

Serve as Consortium and Fred Hutch institutional lead on the CTMS workflow development:

• Provide support and leadership to CTMS implementation and management
• Ensure CTMS operations are in alignment with the business needs of the Consortium

Leadership:

• Represent Clinical Research Support services to study teams, faculty, leadership, and peer institutions
• Identify gaps in Consortium research support; implement new programs and services to address operational gaps
• Represent CRS at Cancer Consortium meetings, committees and performance improvement initiatives
• Identify, champion, and implement process improvement opportunities to Fred Hutch and Consortium executive leadership, by providing sufficient context, data, as well as recommended solutions and resources.

Qualifications

Experience and Abilities

• 5-10 years starting and managing clinical trials operations, preferably oncology
• Managing multi-disciplinary teams
• Communicating with all levels of a research organization
• Working across different academic institutions to facilitate research projects
• Working with multi-disciplinary teams
• Forecasting and meeting deadlines
• Coaching study teams
• Strong understanding of NCI mandates for data reporting and infrastructure
• Using judgment and effective decision making skills with competing interests and priorities

Knowledge and Skills

• Bachelor’s Degree
• Master’s degree healthcare related field preferred
• Clinical research related certification preferred
• Familiarity with process improvement principles
• Familiarity with project management tools and techniques
• Strong verbal and written communication skills
• Knowledge of the regulatory environment surrounding clinical trials

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The CTMS Program Office is a tri-institutional office housed within the Fred Hutch Research Administration department providing implementation and operational support services for the OnCore Clinical Trial Management System (CTMS) that is jointly managed by the Fred Hutch, the University of Washington and the Seattle Cancer Care Alliance (SCCA.)

The CTMS Functional Lead position is a leadership role within the CTMS Implementation team and will be accountable to manage activities and outcomes related to the functional workflow design, testing and workflow documentation for the remainder of the CTMS Implementation. The role will require expert-level analysis skills, project management skills, team and stakeholder management skills. The role will report to the CTMS Project Director and closely collaborate with the technical lead, change management lead and data migration lead to help ensure cross-workstream alignment of functional workflow design with data migration, technology and organizational adoption.

Responsibilities

CTMS Functional Design & Testing

• Define approach for CTMS detailed functional design, convene stakeholder groups and facilitate design activities
• Effectively prepare for and facilitate design meetings and presentations with a diverse range of stakeholders including study coordinators, regulatory coordinators, fiscal coordinators, administrative office staff and leadership
• Develop deep understanding of institutional workflows related to the clinical research administrative offices and study teams
• Work with SMEs and analysts in related systems such as the Epic EHR system to functionally define, test and implement data flows from the CTMS into Epic
• Demonstrate expert-level understanding of the capabilities of a CTMS, specifically OnCore from Forte Systems, to enable efficient workflows for research study teams and administrative offices
• Establish functional testing and user acceptance testing approach and manage testing process
• Manage functional and workflow analysts who will perform testing activities along with super users.
• Design highly accurate and comprehensive functional cutover plans, conduct go-live dress rehearsals and perform cutover activities
• Provide go-live support to end users, and effectively transition functionality from implementation to operations

Project Management

• Define detailed workstream-level project plan for the functional workstream outlining design activities, documentation activities, testing and stakeholder engagement activities and deliverables
• Assign functional workstream tasks, manage workload, inspect workstream deliverables and report workstream status
• Actively manage workstream level risks and issues escalating as needed to project director

Cross-Workstream Collaboration

• Partner with data migration team to define backload strategies that align with future state functional workflows
• Define and implement plans for pre-go-live data validation of migrated data with study teams and administrative offices
• Provide clear and concise information to the training team and change management teams to support the development and delivery of training and adoption sessions

Qualifications

• Bachelor’s Degree
• Minimum five (5) years of experience in clinical research operations
• Prior experience implementing OnCore financials at large, complex institutions
• Experience with IRB systems and workflows is desirable
• Experience working with CTMS integrations related to the Epic EHR system
• Knowledge of applicable industry standards and best practices for clinical research
• Advanced knowledge of business analysis tools, methodologies and best practices; including but not limited to leading cross-functional team discovery and business requirement sessions, process mapping and SWOT analysis
• Proven ability to lead an implementation workstream serving both as project manager and content expert for the functional workstream
• Experience with system conversion, customization and integration design and execution
• Proven ability to communicate complex workflow issues to administrative offices and study team staff
• Sustained, proven ability to think analytically, problem solve and use independent judgment
• Excellent communication (written and oral), customer service, collaboration, problem solving and interpersonal skills
• Superior presentation and organizational skills with an attention to detail mindset
• Proven ability to work with a diverse group of stakeholders, including technical and non-technical personnel at various levels in the organization
• Proven ability to teach and train others

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The CTMS Program Office is a tri-institutional office housed within the Fred Hutch Research Administration department providing implementation and operational support services for the OnCore Clinical Trial Management System (CTMS) that is jointly managed by the Fred Hutch, the University of Washington and the Seattle Cancer Care Alliance (SCCA).

The CTMS Study Financial Management Adoption Lead is a leadership role within the CTMS Implementation team and will be accountable to manage activities and outcomes related to process improvement, change management, operational readiness, and adoption related to the remainder of the CTMS Implementation. The role will require expert-level analysis skills, expert-level understanding of clinical research administration workflows, project management skills, team and stakeholder management skills. The role will report to the CTMS Project Director and closely collaborate with the functional lead, technical lead, change management lead and data migration lead to help ensure cross-workstream alignment of change management and adoption with functional design, data migration, and technology.

Responsibilities

Process Analysis & Improvement

• Actively engage study teams and research administration central offices to understand study financial management workflow pain points and identify improvement opportunities that can be introduced as part of a CTMS implementation.
• Demonstrate expert-level understanding of workflow best practices for study budget management, coverage analysis, coding/pricing, subject visit tracking and sponsor invoicing and champion the alignment of institutional practices with best practices where applicable
• Develop deep understanding of institutional workflows related to the clinical research administrative offices and study teams
• Effectively prepare for and facilitate workflow assessment meetings and presentations with a diverse range of stakeholders including study coordinators, regulatory coordinators, fiscal coordinators, administrative offices staff and leadership
• Engage closely in functional design session planning, facilitation and follow-up to help ensure pain points and improvement opportunities are being appropriately addressed during CTMS design

Change Management, Communication & Training

• Define overall change management strategy and plan including training approach, communication approach, operational cutover approach and adoption approach
• Define training plan for onboarding administrative offices and study teams to new CTMS workflows; oversee development of training materials and training execution
• Define communication strategy and partner closely with communications lead on execution
• Execute change management strategy including leading roadshows, brown bags, adoption sessions, demos, and other forums that help champion the CTMS to a diverse set of stakeholders
• Define and manage the change management governance structure including super user working groups, change champion networks and other such bodies

Project Management

• Define detailed workstream-level project plan for the adoption/change management workstream outlining workflow analysis activities, communication activities, training activities, documentation activities, stakeholder engagement activities, operational cutover activities and deliverables
• Assign adoption/change management workstream tasks to project team members, and manage progress to completion
• Actively manage workstream level risks and issues escalating as needed to project director

Qualifications

• Bachelor’s Degree
• Minimum five (5) years of experience in clinical research operations
• Prior experience with study financial management process improvement at large, complex institutions
• Experience working with CTMS, preferably OnCore from Forte systems
• Knowledge of applicable industry standards and best practices for clinical research
• Advanced knowledge of business analysis tools, methodologies and best practices
• Proven ability to lead an implementation workstream serving both as project manager and content expert for the change management/adoption workstream
• Proven ability to communicate complex workflow issues to administrative offices and study team staff
• Sustained, proven ability to think analytically, problem solve and use independent judgment
• Excellent communication (written and oral), customer service, collaboration, problem solving and interpersonal skills
• Superior presentation and organizational skills with an attention to detail mindset
• Proven ability to work with a diverse group of stakeholders, including technical and non-technical personnel at various levels in the organization
• Proven ability to teach and train others

The Fred Hutchinson Cancer Research Center is seeking a candidate in cancer epidemiology for a faculty position at the Assistant or Associate Member (equivalent to Assistant or Associate Professor) level. We invite candidates whose research is focused on the etiology of cancer and/or cancer survivorship. Areas of particular interest are integrated tumor epidemiology, biomarker research, genetic epidemiology, pharmacoepidemiology, and use of novel data sources (e.g. mobile technology, electronic health records).

Applicants should have a doctoral (PhD or MD with MPH/MS) degree or equivalent training in cancer epidemiology (or a related discipline) and relevant research experience. Candidates will have the opportunity to develop an independent research program within our collaborative, multidisciplinary environment with the focus on cancer prevention and translation.

Fred Hutch’s Division of Public Health Sciences is home to an extensive portfolio of population sciences research, large biospecimen and data repositories, a SEER cancer registry, a prevention center designed for intervention research, and a large multidisciplinary faculty. Fred Hutch, together with the University of Washington, Seattle Children’s, and the Seattle Cancer Care Alliance, is an NCI-designated Comprehensive Cancer Center with active training programs for graduate students and postdoctoral fellows. Opportunities exist for joint and/or affiliate appointment in Fred Hutch’s Divisions of Clinical Research, Human Biology, Basic Sciences, or Vaccine and Infectious Disease, as well the University of Washington, depending on mutual interest.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here. 
 
The primary responsibility of a Cellular Production Associate is to execute manufacturing operations in the production of modified cellular products for patients participating in Fred Hutchinson Cancer Research Center cell therapy clinical protocols. Clinical manufacturing in the Cell Processing Facility (CPF) requires following applicable current Good Manufacturing Practices (cGMP) in a cleanroom processing environment.  

Responsibilities

1. Utilizing aseptic techniques, perform a variety of open cell product manipulations in an ISO 5 biosafety cabinet. 
2. Follow Standard Operating Procedures (SOPs) and complete required processing documentation such as production batch records.  
3. Perform cell processing operations such as cell selection/depletion, expansion, stimulation, transduction, cryopreservation, and preparing patient infusions. 
4. Develop capability in review of executed GMP process documentation. 
5. Submit deviation documentation and assist with investigations of nonconformance. 
6. Maintain and operate primary process equipment, such as incubators, centrifuges, cell sorting/selection equipment and controlled rate freezers. 
7. Participate in problem solving and troubleshooting of cell processing operations and equipment. Assist in the evaluation of current practices and operations and help to implement changes to improve performance. 
8. Participate in Corrective and Preventative Actions (CAPA) development
9. Participate in quality/compliance improvement and technical development projects supporting manufacturing. 

 
We are open to considering candidates of multiple experience levels and encourage you to apply if interested. A more experienced individual may have the opportunity to take on the following responsibilities:  

1. Perform routine review of executed GMP process documentation. 
2. Submit deviation documentation and complete deviation investigations and reports.  
3. Take an active role in problem solving and troubleshooting of cell processing operations and equipment. Evaluate current practices and operations and implement changes to improve performance. 
4. Participate in Corrective and Preventative Actions (CAPA) development and completion, and GMP Systems change control. 
5. Provide guidance and training to junior staff. 
6. Work with Process Engineering and GMP Systems to lead equipment on-boarding and validation projects. 
7. Act as Protocol Champion, assigned to specific clinical protocols as a point of contact for manufacturing readiness and execution, reporting out production status and production run summary data as needed. 
8. Lead by example and take responsibility in the support of safety and cGMP compliance. 

Qualifications

Minimum:  

1. Bachelor’s degree in a biological science, or equivalent cGMP manufacturing bioprocessing experience. 
2. Experience with open aseptic processing, working in biosafety cabinets. 
3. Experience with fundamentals of cell culture preferred. 
4. Must be able to work efficiently, with strong attention to detail in a highly regulated environment. 
5. Computer skills highly desirable (MS Office). 
6. Must be able to support and communicate effectively in a diverse team environment. 
7. Must demonstrate solid time management and organizational skills, and good verbal and written communication. 
8. Must be able to wear appropriate clean room attire and have the ability to wear surgical masks and all required Personal Protective Equipment (PPE). 
9. Must have the ability to stand for long periods. 
10. Meets physical requirements of the job, as follows:  must have the ability to lift a minimum of 50 pounds, the ability to bend, reach, stretch, climb ladders and work in tight spaces in order to complete job tasks.
11. Ability to work non-standard shifts and occasional weekend days or evenings. 4/10 Shifts: Sun-Wed 7AM-5:30PM, Mon-Thurs 11AM-9:30PM, Tues-Fri 7AM-5:30PM (current opening). The current opening is available on the Tues-Fri shift, however we will consider interest in alternate shifts and encourage you to apply if interested.  

Preferred:  

1. A minimum of three years' experience as a production associate for Cell Therapy product production. 
2. Mastery of open aseptic processing, working in biosafety cabinets. 
3. Experience with cell culture.  Establishing and maintaining long-term T-cell lines/clones preferred. 
4. Experience writing or revising standard operating procedures, manufacturing batch records, and other GMP Systems documentation. 

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The Cellular Therapy Lab (CTL) at the Seattle Cancer Care Alliance (SCCA) is on the cutting edge of new technologies for cancer therapy, including cell-based immunotherapy. We are committed to advancing treatment options for our patients through the translation of innovative research into clinical practice. We collaborate with our Alliance members (University of Washington, Fred Hutchinson Cancer Research Center and Seattle Children’s Hospital) as well as corporate entities. CTL is responsible for all minimally manipulated therapeutic cell processing occurring at the SCCA. Procedures range from cryopreservation to flow cytometric enumeration of cell proportions to more complex procedures such as cell selection, enrichment, and depletion. The laboratory is regulated by the FDA cGTP/cGMP standards, maintains CAP certification, and is accredited by the Joint Commission and FACT.

We currently have an opening for a Cellular Therapy Technologist II. This a full-time position (40 hours per week). This position requires a flexible schedule that can include on-call, evenings, weekends, and holidays.

Responsibilities

• Process cellular products/specimens according to standard operating procedure (SOP), and specific guidance for clinical trials, using aseptic technique.
• Perform and analyze results of quality control testing of components, including automated nucleated cell counts and flow cytometry
• Document processing steps accurately, generate processing reports and prepare patient/donor laboratory charts; review processing reports and charts
• Understand and stay current with SOPs as needed, and perform SOP qualifications. Provide input/feedback to Lab Supervisor on documentation and process improvements
• Thaw cryopreserved components and assist with infusion at the patient bedside
• Meet unrelated donor (URD) component couriers and perform necessary testing and processing of components prior to release
• Potentially assist with the bone marrow collection within operating rooms
• Perform clinical trials processing:
  • CliniMACS® cell selection e.g. CD34+ cell enrichment, CD3+ cell depletion
  • CAR-T therapy processing and cryopreservation

Qualifications

Required:

• Four-year college degree with major in biological science or related degree
• Basic hematology knowledge
• Motivation and initiative to learn new scientific theory and applications
• Mature judgment
• Work independently
• Proven team player
• Collaborate and communicate effectively across functions
• Interpret data thoroughly
• Strong trouble-shooting capabilities
• Scientific writing skills, including preparation of clear, concise SOPs and technical reports
• Strong math skills
• Strong communication skills
• Attention to detail
• Flexibility in scheduling: night, weekend, holiday and on-call rotations

Preferred:

• 2+ years of clinical cell therapy experience
• Advanced knowledge of oncology, hematology and/or immunology
• Flow cytometry expertise
• Immunotherapy experience
• CliniMACS® operation experience
• Surgical tech experience
• LabWare LIMS knowledge
• A good understanding of cGMP/cGTP standards
• Proven record of completing projects efficiently and effectively

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The Spiritual Health department at the SCCA provides relationally-grounded, outcomes-oriented, multidisciplinary, and research-informed chaplaincy care to culturally and spiritually diverse patients, family, and staff, both inpatient (at UW Medical Center) and outpatient (at the SCCA— South Lake Union, SCCA--Northwest Hospital campus, and SCCA—Peninsula/Poulsbo). Spiritual Health embraces continuous quality improvement, a culture of learning and engagement, and professional leadership in the oncology and outpatient chaplaincy arenas. The department is engaged in clinical care, education, and some research

The SCCA has an opening in Spiritual Health for a full-time position (5 days per week), primarily in the outpatient setting (e.g., 4 days per week) but with some regular inpatient responsibilities (e.g., 1 day per week). Responsibilities include provision of care to adults with cancer as well as to their support persons and to staff. The ideal candidate will:

• have demonstrated chaplaincy care skills
• work well both independently and with colleagues (e.g., within a department of five and with health care teams)
• function well in a complex academic medical specialty care context
• demonstrate good analytical skills and attention to detail
• evidence strong capabilities with electronic charting and Microsoft Office and exhibit proficiency in thorough documentation of clinical work
• thrive in an environment of ongoing change, both in healthcare services delivery and in chaplaincy care.

Responsibilities

• Screen and assess patient/family needs, resources, struggles, hopes, and goals
• Actively, empathically, and compassionately inquire and facilitate conversation, rituals, and connections around these issues, intervening in ways that sustain, guide, and/or work toward healing
• Explore life histories, legacies, and values/goals that guide medical decisions and that help patients/families navigate challenging times in meaningful and potentially transformative ways
• Provide care, counsel, debriefings, and specialized programs to support staff, providers, volunteers, non-employees at all sites of care
• Educate staff, providers, students, and volunteers regarding spiritual, religious, emotional, and existential issues as well as how to collaborate in screening for and addressing these issues
• Be a voice for the spiritual, religious, and emotional needs and well-being in the broader organization
• Be active participants in relationally-grounded, evidence-based, research-informed chaplaincy care that seeks continuous quality improvement

Qualifications

Application instructions:

To apply and be considered for the position please submit a formal electronic application on our careers site. Please be prepared to include all of the following: a cover letter, including reason for applying, and a resume. Also, please e-mail a verbatim account of one of your chaplaincy care encounters (and analysis) reflecting your current abilities to The Rev. Stephen King, Ph.D, at sking@seattlecca.org. For full consideration, please apply by November 15th.

Required:

• MDiv or equivalent degree appropriate for certifications below; at least four units of clinical pastoral education (ACPE)
• Religious group endorsement for health care, all leading to certification in the Association of Professional Chaplains or equivalent organization sharing common standards within two years
• Ability to communicate effectively with culturally, religiously, and spiritually diverse patients, providers, families, staff, volunteers, non-employees
• Demonstrates professional values and behaviors, demonstrates good boundaries, demonstrates good leadership skills, remains non-judgmental , and respects the dignity and worth of every individual
• Must have excellent chaplaincy care skills, work well independently and with others, function well in complex and constantly changing contexts, be committed to continuous improvement, have good analytical skills, be a detail-oriented person, and work well with electronic charting and Microsoft Office
• Must be committed to learning and providing outcomes-oriented, evidence-based chaplaincy care, and have a strong desire to becoming research literate in the field

Preferred:

• Education or experience in a major academic health care organization
• Substantial experience in oncology
• Knowledge regarding spiritual/religious/existential distress and negative spiritual/religious coping

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. The Center’s five scientific divisions collaborate to form a unique environment for conducting basic and applied science. Vaccine and Infectious Diseases Division (VIDD) works to eliminate or minimize the impact of globally significant infectious diseases. Within VIDD is the Statistical Center for HIV/AIDS Research & Prevention (SCHARP), which provides statistical support and data management to researchers worldwide in the fight against HIV/AIDS with active studies in the U.S., Africa, Latin America, Asia and Europe. Careers Start Here.

The Statistical Center for HIV/AIDS Research and Prevention (SCHARP) at Fred Hutch is a full service statistical and data management center focused on HIV prevention research. SCHARP has an annual budget of over $40 million, more than 180 employees and is currently managing over 40 active phase I – III clinical trials in over 150 clinical sites around the world. SCHARP is seeking a Clinical Coding Specialist. The specialist is responsible for abstracting and coding Adverse Events (AEs) and Concomitant Medications (ConMeds) information from clinical trials data using the Medical Dictionary for Regulatory Activities (MedDRA) and WHO Drug Dictionary (WHO-DD) tools. Assists in coordinating the collection and entry of study site-specific laboratory reference ranges. Depending on experience, may also assist in the management of the lab normal range database and train and mentor junior staff.

Responsibilities

The incumbent works with limited supervision in performing daily work assignments.

1. Using the clinical coding tools and other established SCHARP guidelines, select the clinical code most closely aligned with the adverse event being reported.
2. Review reported AE and ConMeds to identify inadequate, ambiguous or unclear medical terms/medications and generates coding queries as necessary.
3. Manages queries related to coding terms, through closure; including entering queries into EDC and triaging site or Medial Monitor questions.
4. Review coded data to ensure coding is both correct and codes are applied consistently across all studies in accordance with established work instructions.
5. On request, assist other members of the Clinical Coding & Safety staff or SCHARP staff with information from the MedDRA and WHO-DD Coding tools.
6. Participate in MedDRA and WHO-DD trainings to remain up to date on procedural and coding changes, as well as standard industry practices.
7. Participate on SCHARP working groups and special projects, as needed.
8. Assists in coordinating the collection and entry of study site-specific laboratory reference ranges.
9. Conduct all job duties within context of Good Clinical Practice (GCP) and according to SCHARP SOPs and guidelines.
10. Works mostly independently on daily activities with minimal instruction. Exercises good judgment within scope of responsibilities to determine appropriate actions.

Qualifications

Minimum:

• Bachelors or higher required, in related field desired
• Minimum of 2 years of Data Management experience in clinical trials
• Minimum of 1 year of experience performing clinical coding in clinical trials and knowledge of MedDRA and WHO Drug coding practices
• Familiar with Clinical Coding Dictionaries (MedDRA and WHO Drug) and best Clinical Data Management practices
• Knowledge of and experience with clinical coding dictionaries and terminology
• Familiarity with GCP, ICH and FDA requirements as they apply to clinical data
• Demonstrated technical skills (EDC systems, MS Excel, Word, PowerPoint), Medidata Coder and Medidata Lab Admin experience desired
• Regular interaction with Data Management Groups
• Excellent written and oral communication skills
   

Preferred:

• 4+ years of Data Management experience in clinical trials.
• 3+ years of experience performing clinical coding in clinical trials and knowledge of MedDRA and WHO Drug coding practices
• Fully conversant of Clinical Coding Dictionaries (MedDRA and WHO Drug) and best Clinical Data Management practices
• Knowledge of and experience with developing and maintaining coding guidelines, quality control processes and auditing procedures.

Overview

Seattle Cancer Care Alliance (SCCA) brings together the leading research teams and cancer specialists of Fred Hutch, Seattle Children’s, and UW Medicine. One extraordinary group whose sole mission is the pursuit of better, longer, richer lives for our patients. SCCA's purpose is to provide state-of-the-art, patient and family centered care; support the conduct of cancer clinical research and education; enhance access to improved cancer interventions; and advance the standard of cancer care regionally and beyond.

Every individual at SCCA plays a unique role in supporting our mission. Our collective success hinges on each of us conducting ourselves in accord with a set of core values:

• We are patient-centered. Everything we do must be linked to our ability to deliver better, safer outcomes for our patients.
• We are innovative. We nurture an environment that fosters unconventional thinking, a passion for discovery, and the open-mindedness to invite discovery from unexpected places.
• We are respectful. We are deeply respectful of our patients, their families, and each of our colleagues who serve them in so many different and important ways.
• We are collaborative. We understand that asking for and offering help in how to do better is not just a right, but among our most important responsibilities.
• We are agile. We cannot just be comfortable with change; we must embrace it as proof that we are making progress.
• We are responsible. Because our work is focused on people's well-being, we approach it with the highest level of ethical, fiduciary, and environmental responsibility.

This is an extraordinary opportunity to lead disruptive continuous innovations in the fight against cancer.

Responsibilities

The Unit Attendant is responsible for the pick-up, transportation and delivery of lab specimens, medical records and patient related documentation among various departments within SCCA clinic, on SCCA/Fred Hutch campus and University of Washington Medical Center via shuttle service or by driving an SCCA vehicle

• Pick up, transport and deliver lab specimens, medical records and patient related documentation among various departments and within the SCCA/Fred Hutch campus and University of Washington shuttles or by driving an SCCA vehicle
• Complete all scheduled and requested pickups.
• Monitor courier phone and manage shifting priorities to maintain route schedule.
• Maintain courier logs in pickup/delivery locations and ensure courier entries are legible, accurate and adhere to standard written procedures.
• Report and assist with tracking of missing or damaged specimens and charts.
• Assist with review and revision of routes and training new couriers as needed

Qualifications

Required:

• A High School Degree, GED, or equivalent combination of education and experience.
• Ability to professionally and effective communicate in person and in writing.
• Excellent multi-tasking and interpersonal skills.
• Knowledge of computerized or automated system operations and record keeping practices.
• Basic math skills and knowledge of units of measure.
• Ability to lift up to 50 pounds using proper techniques.
• Ability to work effectively in a fast paced environment.
• Ability to consistently walk during most of eight hour shift, an average of 10-12 miles per day.
• Current Washington State Driver's License
• Current Abstract of Driving Record (ADR), ADR (due upon hire or 30 days post hire).
• Ability to Pass the online Defensive Driving Course (upon hire).

Preferred:

• One year experience. One year experience in a hospital/clinic environment preferred.
• Basic computer skills.
• Knowledge and practice of safe blood borne pathogen handling techniques
• Ability to read and interpret documents such as safety rules, operating and maintenance instructions and procedure manuals and carry out instructions in written, oral or diagram form

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. The Center’s five scientific divisions collaborate to form a unique environment for conducting basic and applied science. Vaccine and Infectious Diseases Division (VIDD) works to eliminate or minimize the impact of globally significant infectious diseases. Within VIDD is the Statistical Center for HIV/AIDS Research & Prevention (SCHARP), which provides statistical support and data management to researchers worldwide in the fight against HIV/AIDS with active studies in the U.S., Africa, Latin America, Asia and Europe. Careers Start Here.

The Statistical Center for HIV/AIDS Research and Prevention (SCHARP) at Fred Hutch is a full service statistical and data management center focused on HIV prevention research. SCHARP has an annual budget of over $40 million, more than 180 employees and is currently managing over 40 active phase I – III clinical trials in over 150 clinical sites around the world. SCHARP is seeking a Clinical Data Manager (CDM).

The CDM leads and monitors the collection, processing, data entry and quality control of study data. They are responsible for effectively managing timelines, quality and delivery of data for assigned projects that are in support of clinical trials research. They develop and maintain successful working relationships with their team and specific research sites to ensure and maintain data integrity and quality. The CDM works within a network/study/protocol team to support the policies and goals of each project assigned. Applying GCP and GCDMP principles, the CDM manages the protocol/study specific tasks including coordinating clinical and laboratory database deliverables, working with collaborators on data content requirements, leading data quality and closeout activities throughout the data management lifecycle. The CDM adheres to SCHARP Standard Operating Procedures (SOPs), Work Practice Guidelines (WPGs), applicable clinical trial regulations, and study confidentiality requirements and functions with moderate supervision in operational and technical matters within defined procedures and practices.

**Please note: This position will be on-site in Seattle, WA. We cannot accommodate a remote worker in this role at this time.

Responsibilities

The Clinical Data Manager (CDM) will manage study/protocols with moderate supervision from senior staff and/or departmental leadership and will use judgment in making decisions regarding routine data management, quality control and liaison tasks. The CDM is the primary SCHARP contact for study/protocol specific implementation, operation, and closeout phases and is responsible study communication, documentation, and training on data collection and management activities for domestic and international research sites for assigned protocol/study(s).   The CDM is a member of the protocol/study team coordinating with both internal and external partners and collaborators to ensure the relevant data are collected and cleaned to meet the needs of the protocol/study and research objectives.

For the more experienced CDM, they may participate in training and orientation of new CDMs when appropriate, and may serve as a CDM mentor. Assignment of projects/trials is commensurate with previous experience and can be assigned across scientific areas or study phases. They will be coordinating larger, more complex studies and/or a larger volume of studies with minimal assistance.

• Manages study/project implementation including but not limited to leading SCHARP team members through CRF, lab, and other data collection processes, reporting and analysis requirements, study/project documentation and training.
• Effectively manage assigned protocol/study, establish timelines and milestones, monitor and communicate ongoing status and progress.
• Ensure rapid resolution of issues/problems using appropriate internal and/or external resources. Track and manage issues escalating to the appropriate level in a timely manner.
• Participate in development of protocol/study from draft protocol to optimize collection of accurate and high-quality data.
• Work with project sponsors, stakeholders and SCHARP team members to define project requirements, scope, risks, staffing requirements, organization and approach.
• Act as subject matter expert for data management issues between SCHARP study teams and external domestic and international research sites for assigned studies.
• Assist in development of Case Report Forms (CRFs) for assigned studies.
• Assist in the design of the protocol/study specific database for assigned studies.
• Assist in the maintenance of the study database including routine revisions or additions to include the design and/or modification of routine and existing study database edit check programs for assigned studies.
• Perform User Acceptance Testing (UAT) for assigned studies.
• Monitor study data to insure the quality and completeness of the data submitted by implementing quality control procedures.
• Generate QC reports for site review and correction as well as a variety of other reports as required.
• Evaluate study data for protocol compliance.
• Assist in the maintenance of documentation of the study database and other related data management programs and/or applications.
• Assist in the review of new and revised departmental SOPs and WPGs.
• Ensure that SCHARP meets its obligations in accordance with Good Clinical Data Management Practices (GCDMP).
• Perform other duties as assigned.

Qualifications

Minimum:

• Bachelor’s degree or equivalent, preferably in a health-related or scientific discipline
• 2+ years’ experience in the pharmaceutical/clinical research environment as a Clinical Data Coordinator/Clinical Data Manager
• EDC experience required. Working knowledge of Medidata Rave highly desirable. Demonstrated expertise in relevant clinical data management activities.
• Working knowledge of ICH/GCP guidelines and FDA regulations.
• Familiarity with all phases of clinical trials and ability to adapt to study requirements.
• Strong verbal and written communication skills. Ability to understand and follow instructions and guidelines; able to pick up new tasks quickly; willing to ask questions when a task is not fully clear.
• Ability to exercise independent judgment within generally defined practices and policies. Shows good judgment in interpreting guidelines and when to seek support.
• Ability to work independently and to work efficiently under pressure. 
• Consistent, dedicated, versatile and able to prioritize and multi-task.
• Familiarity with MS Office software and familiar with data management practices.   
   

Preferred:

• 4+ years' experience in the pharmaceutical/clinical research environment as a Clinical Data Manager.
• Experience using SAS and relational databases (e.g. MS SQL Server, MS Access, or Oracle)
• Experience in clinical trial and regulated research settings desired. Experience with managing immunology, infectious disease and/or virology research projects desired.
• Prior experience in HIV or infectious diseases, clinical trial operation management and/or protocol development preferred.
• Experience in facilitating and building consensus in an interdisciplinary team environment and able to build successful working relationships with a wide variety of collaborators.
• Knowledge of clinical research, FDA & ICH, GCP, GCDMP, and related regulatory requirements

Overview

The Clinical Nurse/Registered Nurse provides and coordinates all clinical aspects of care for patients receiving proton radiation therapy, in collaboration with a multidisciplinary team to achieve predetermined quality outcomes. The Registered Nurse will be expected to perform clinical research tasks that are interrelated to the daily function of the clinic. It will be the responsibility of the Registered Nurse to assure all federal regulations regarding research are followed and work in collaboration with Research. This position requires the ability to work 2 Second Shifts per week, please inquire.

Click HERE to apply for Clinical Nurse

Responsibilities

• Educates patients in the proton therapy clinics; responds to consultations made by physicians.
• Performs patient histories and physical examinations under physician supervision; evaluates results and monitors treatment plans; maintains medical records.
• Oversees patient schedules, appointments, and procedures
• Participates in educational in-services and seminars for health care providers at the ProCure Proton Therapy Center as well as the surrounding area; maintains current certification through continuing education.
• Accountable for the management of patient care in assigned service(s).
• Utilizes critical thinking skills to recognize and solve patient problems.
• Identifies the age specific growth and developmental needs of the patients, and utilizes the nursing process and nursing standards to prevent or manage actual/potential problems in the assigned service of the Proton Therapy Clinic.
• Identifies patient /family nursing needs and assures that they are met.
• Inputs, retrieves, and interprets data from multiple manual and computer information systems.
• Maintains patients rights and demonstrates respect for persons of all ages and diverse cultures.
• Utilizes organizational skills to assure continuity of care in collaboration with other disciplines through appropriate planning, education, and coordination of other services.
• Collaborates with the medical staff to facilitate and optimize patient care.
• Acts on behalf of the patients and family to ensure care that is safe and appropriate with consideration for values, diversity, and human rights.
• Participates in nursing and medical research and facilitates transfer of new knowledge to patient care.
• Ability to have a flexible schedule.

Click HERE to apply for Clinical Nurse

Qualifications

WORK EXPERIENCE REQUIREMENTS

• One year of experience in patient care required
• Two years of oncology experience or pediatric OR/Recovery preferred

REQUIRED SKILLS AND ABILITIES

• Knowledge of medical procedures, terminology, and equipment
• Patient assessment skills
• Ability to apply good clinical judgment
• Ability to plan work, establish priorities, and remain flexible
• Ability to maintain confidentiality
• Knowledge of general nursing principles and practices.
• Knowledge of scientific principles and specialized techniques used in the practice of nursing.
• Knowledge of medications and treatments.
• Knowledge of current literature in the field of nursing and hospital administration.
• Ability to assess the effectiveness of nursing care.
• Ability to maintain records, prepares reports, and composes correspondence.
• Ability to communicate effectively with co-workers, subordinates, superiors, partner hospitals/medical practices, the general public, representatives of public and private organizations and others sufficient to exchange or convey information.
• Able to work evening hours twice a week.

COMPETENCIES

• Problem Solving/Conflict Resolution
• Performance Standards
• Flexibility/Managing Change
• Interpersonal Communication Skills
• Fostering Teamwork

EDUCATION/DEGREE

• Graduate of an approved RN program, with bachelors degree in nursing preferred; supplemented with two years of related clinical nursing experience
• Washington State RN licensure required
• Certification in Basic Life Support (BLS) required
• Certification in Pediatric Advanced Life Support (PALS) preferred

Click HERE to apply for Clinical Nurse

Overview

EXCEPTIONAL CANCER CARE, EXCEPTIONAL NURSES
 
At Seattle Cancer Care Alliance every patient, every life matters. Our dedicated nurses are a driving force making SCCA a global leader in the prevention, treatment, and cure of cancer. Our nurses rank among leading experts in oncology. They integrate patient and family-centered care with support for the research and development of innovative therapies, embarking with each patient on a journey through cancer treatment and survival to ensure the best possible patient outcome. Our nurses are vital to the journey of cancer care. 
 
The Hematology/Oncology clinic has an exciting opportunity for a Clinical Nurse Coordinator (CNC). Join our bright and supportive nursing team that provides comprehensive care management for complex outpatient oncology clients. Work with a dynamic multidisciplinary team where your critical-thinking and problem-solving  skills will be challenged and also valued. Collaborate closely with your care team, including nationally-recognized specialists in Hematology and Oncology, to bring the most innovative therapies to patients.

The Clinics are open weekdays 8:30 AM - 5:00 PM, closed weekends and holidays.  Some flexible scheduling may be possible.  Be part of a team that supports and encourages professional development and fulfillment.  

Benefits include:

• Relocation - Generous relocation package available
• Time Off - 10 paid holidays plus 2 personal days, paid vacation, and paid sick time
• Employee Health Clinic - Onsite employee health clinic services are free for employees enrolled in a Kaiser or Premera Blue Cross plan 
• Retirement - 403(b) defined contribution plan with a 7% employer contribution after 1 year and 1000 hours of service
• Bright Horizons Care Advantage  
• Hutch Kids Child Care Center 
• Employee Assistance Program 
• Tuition Reimbursement Program   
• Subsidized ORCA card and tax-advantaged transportation options 

Responsibilities

The CNC provides clinical support to medical providers, providing care management to their entire panel of patients. As the primary point of contact for complex outpatients, the Heme CNC provides continuity of care through nursing assessments, triage, patient education and care coordination. The clinical nurse coordinator is an integral part of a dedicated multidisciplinary team which collaborates closely to provide the highest level of care for patients.  In this position you will:  

• Establish long-term relationships with patients and families as you help them navigate their disease and treatment
• Assess patient and family needs along the continuum of care from diagnosis, treatment, to survivorship
• Act as primary point of contact for patients/caregivers to provide education, triage and symptom management,  in-person and on the phone
• Coordinate care within our SCCA/UW Medical Center facility as well as with outside healthcare facilities
• Monitor the health status of complex patients and collaborate with multidisciplinary care teams to provide the highest and safest level of care

Qualifications

Required:

• Nursing degree
• Current Washington State Registered Nurse license
• Current BLS AHA Health Provider Card (or equivalent course, such as by the American Red Cross) and renewal required every two years
• Minimum one year inpatient hospital experience
• Excellent communication skills
• Excellent assessment skills
• Ability to perform triage both in-person and by phone
• Ability to work under pressure
• Competence in basic computer skills

Preferred:

• Bachelor of Science in Nursing
• Oncology experience
• OCN Certification

Overview

EXCEPTIONAL CANCER CARE, EXCEPTIONAL NURSES

Seattle Cancer Care Alliance, in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. These three organizations have worked together to support their mission of world class adult and pediatric oncology patient care services, research and education. Please join us and be part of making a difference in the lives of our patients, families, and community!

At Seattle Cancer Care Alliance every patient, every life matters. Our dedicated nurses are a driving force making SCCA a global leader in the prevention, treatment, and cure of cancer. Our nurses rank among leading experts in oncology. Our nurses provide exceptional patient and family-centered care as they coordinate and assist in individualized treatment. They integrate care with support for the research and development of innovative therapies. Embarking with each patient on a journey through cancer treatment and survival, our compassionate nurses walk hand-in-hand with courage and hope with each individual to ensure the best possible patient outcome. 

Our nurses are vital to the journey of cancer care. We invite you to explore our career opportunities and apply online for more information.

Benefits include:

• Relocation - Generous relocation package available
• Time Off - 10 paid holidays plus 2 personal days, paid vacation, and paid sick time
• Employee Health Clinic - Onsite employee health clinic services are free for employees enrolled in a Kaiser or Premera Blue Cross plan 
• Retirement - 403(b) defined contribution plan with a 7% employer contribution after 1 year and 1000 hours of service
• Bright Horizons Care Advantage  
• Hutch Kids Child Care Center 
• Employee Assistance Program 
• Tuition Reimbursement Program   
• Subsidized ORCA card and tax-advantaged transportation options 

Responsibilities

The Registered Nurse for the Gastrointestinal Clinic provides longitudinal comprehensive nursing care to GI oncology patients. This position serves as a primary point of contact for patients receiving treatment with a medical oncology provider. They will be responsible for coordination of care, education of patients and caregivers, triage, and support of providers.

Care Coordination

The Clinical Nurse Coordinator for this population should be able to effectively coordinate patient care through:

• A high level understanding of gastrointestinal cancers and treatment modalities
• Telephone triage
• Development of a plan of care
• Management of prescription refills, prior authorizations, and home health
• Monitoring of patient response to therapies in collaboration with medical, nutrition, and pharmacy staff
• Management of ongoing physical, emotional, and social needs of patients through continuous assessments of adaptation to illness

Patient and Family Education

• Maintains primary responsibility and coordination for provision of education required for patient and family
• Will be expected to develop good knowledge base of chemotherapy regimens
• Provides patient education prior to new chemotherapy/biotherapy regimens and symptom management

Triage

• Responsible for triaging patients in clinic as well as over the phone and via electronic communication

Communication and Teamwork

• Demonstrates effective verbal and written communication skills
• Able to collaborate effectively with physicians to provide comprehensive care planning for their specific population of patients
• Serves as resources in their areas of expertise for other staff
• Demonstrates ability to effectively intervene with a patient in crisis

Qualifications

Required:

• Nursing degree
• Current Washington State Nursing License
• Current BLS AHA Health Provider Card
• One year of nursing experience

Preferred:

• BSN
• Oncology experience
• Outpatient experience
• Nursing Certification (i.e., OCN, ACNC)

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

Reporting to the Clinical Pathways Manager, the Clinical Pathway Associate (CPA) is responsible for coordinating and facilitating the development of clinical pathways with cross functional teams, the integration of pathways into daily clinical operations and the reporting of pathway concordance. The ideal candidate has a background in healthcare with excellent interpersonal skills, an analytical mindset, and experience managing projects and/or in process improvement.

The Clinical Pathways Associate is an important member of a multi-departmental team focused on supporting the SCCA’s organizational priorities and achieving the SCCA’s mission.

Responsibilities

• Manage the lifecycle of clinical pathways (development, implementation, maintenance, reporting)
• Manage a portfolio of 10 or more clinical pathways across various disease groups
• Develop new pathways for disease types not currently represented in the pathway’s portfolio
• Ensure the bi-annual maintenance of “in practice” pathways is completed
• Facilitate the ongoing delivery of reports to medical providers, leadership, and other stakeholders
• Manage data in the Pathways Abstraction Reporting Tool
• Work in close collaboration with Clinical Pathway stakeholders such as Service Line Management, Quality and Clinical Analytics
• Facilitate working group meetings to maintain the integrity of the clinical pathway content
• Schedule meetings with providers and other allied health team members involved in pathway development, maintenance, and reporting work
• Build relationships and collaborations with community site partners to ensure the standard of care is happening across all community sites

Qualifications

Required:

• Bachelor's degree and/or a minimum of four (4) years of equivalent healthcare work experience
• Proficient with Microsoft Project, Excel, Visio, and other Office 2010 & 2013 applications
• Strong technical writing and process documentation experience required
• Demonstrated group facilitation and presentation skills, with the ability to communicate effectively with a wide variety of individuals and groups
• Excellent time management, task prioritization and organizational skills with demonstrated experience in managing multiple projects and coordinating the activities of various resource pools
• Excellent communicator with strong customer focus. Ability to communicate clearly, effectively and concisely to a variety of audiences.
• Broad expertise and project management knowledge, with skills to achieve goals in creative, innovative and effective ways
• Ability and experience working in ambiguous and dynamic environments
• Strong attention to detail in all efforts

Preferred:

• Master's degree in a related field and/or 5+ years of equivalent work experience. A degree in nursing, health care administration or business preferred
• Knowledge of hospital and healthcare systems and/or experience in an academic center
• Strong combination of technical and business skills acumen. Product/Program Managers are good examples
• Experienced in developing and maintaining documentation templates and creating project specific deliverables
• Demonstrated ability to determine the key business issues and develop appropriate action plans from multidisciplinary perspectives
• Demonstrated ability to conduct and interpret quantitative/qualitative analysis
• Proven leadership skills in leading cross functional project management and consulting initiatives
• Experience directly working with physicians and other clinicians

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Clinical Research Compliance Manager is responsible for ensuring clinical research is conducted according to the highest quality standards and in compliance with local, state and federal regulations. The Compliance Manager reports to the  Assistant Director of Regulatory Affairs and Compliance in the clinical trials office, Clinical Research Support (CRS), for the Fred Hutch/University of Washington Cancer Consortium. The position collaborates with partner institutions, Office of General Counsel, Institutional Review Office, Division Administrators, Clinical Research Management and Training.

Responsibilities

Please include a cover letter with your application detailing your interest and qualifications for this position.

• Prepares and implements remediation and corrective action plans, audits response timelines and escalation plans; communicates expectations in a collaborative environment
• Conducts for-cause and spot audits of clinical trials
• Develops, implements and maintains Compliance policies and standard operating procedures
• Assesses resources and needs to meet NCI-Designated Cancer Center guidelines and Center strategic planning goals
• Acts as primary Institutional contact for compliance and regulatory-related communications with outside sponsors, partners and regulatory institutions
• Participates in Consortium study review committees
• Coordinates with Regulatory Affairs team when needed to address regulatory-related matters
• Defines compliance and quality metrics, performs qualitative and quantitative data analyses and reports findings to senior management
• Assists with the development of standard training requirements and assists with ongoing compliance-related education and training for investigators and research personnel
• Identifies compliance risks during study start-up and management; works directly with investigator and research personnel to define root causes and recommend areas of training and process improvements
• Collaborates with partner institutions to facilitate start-up, management and audit of clinical research activities that are compliant with guidelines and regulatory requirements including billing compliance
• Maintains visibility and awareness of the roles and resources available; represents the Program at presentations, meetings and other out-reach activities for Cancer Consortium faculty and research personnel
• Participates in Center-wide and Cancer Consortium process improvement projects and leads quality-related improvement projects

Qualifications

• Bachelor’s Degree; Master’s Degree in health care related field preferred
• Three to Five (3-5) years working experience in a research quality and/or auditing environment with expertise, knowledge, and GCP experience in auditing clinical trials, including auditing internal processes, performing sponsor audits, and proficiency with electronic systems used to manage clinical trial data or safety reporting. Oncology and/or hematology research experience preferred.
• Assessing risk in the conduct of clinical research
• Communicating with all levels of a research organization
• Interpreting federal regulations and guidelines
• Designing tools for the management of clinical research
• Developing corrective action plans for study teams
• Working across large academic institutions
• Thorough understanding of the regulations governing human subjects research
• Clinical research and compliance certification preferred

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

We are looking for a Clinical Research Coordinator to join our dynamic and growing team of dedicated and skilled research staff working on clinical trials in the field of hematologic malignancies. The Clinical Research Coordinator will participate in the planning, coordination, and implementation of multiple industry- sponsored and investigator-initiated clinical trials involving human subjects. This individual will work under the supervision of the Clinical Program Operations Director and will be required to perform their responsibilities with a high level of independence within the scope of study protocols and institutional guidelines.

Responsibilities

• Serve as designee of the Principal Investigator (PI) to manage the daily clinical operations of assigned research studies in accordance with regulatory, GCP guidelines and institutional policy
• Review study candidates’ medical records in detail for study eligibility
• Ensure informed consent, initiate patient enrollment, and ensure accurate enrollment records are maintained
• Educate clinical teams, ancillary departments, and patients to ensure safe and accurate protocol implementation
• Develop and maintain tools for study implementation, which may include data collection tools, study reference materials, and study specific orders.   Revise and utilize tools as necessary to fulfill the aims of the clinical trial.
• Initiate scheduling of patient clinic visits, and on-going study visits.  Attend patient visits and ensure clinical procedures, lab test, and other protocol specific activities are completed as outlined in the protocols.
• Complete requisition forms, assemble kits for upcoming research visits, transport laboratory samples, and ensure samples are processed and shipped according to study specific guidelines, while tracking and maintaining research supplies
• Collaborate with Investigational Drug Services (IDS) on drug assignment, dispensation information, and maintain regular communication regarding status of study subjects
• Ensure study drug self-administration and accountability with patients, perform non-clinical ECGs, administer study questionnaires and other protocol-driven non-clinical assessments
• Function as a protocol liaison with clinical teams, patients, and when necessary, other institutions or drug companies
• Maintain appropriate source documentation, and complete or assist with accurate data entry into case report forms in a timely manner.
• Coordinate monitoring/auditing visits and respond to queries and other requests from study monitors/auditors
• Identify, documents, and report adverse events in accordance with protocol, regulatory guidelines, and institutional policy
• Understand clinical trial budget and billing plans for patients enrolled on clinical trials. Participate in the review of charges for patients on clinical trials to ensure billing compliance.
• Provide input regarding IRB correspondence and regulatory documentation
• Travel for industry sponsored investigator meetings
• Maintain thorough knowledge in the field through attending related project meetings and symposia, reading related literature, and maintaining professional associations
• Provide back up for other Clinical Trial Coordinators as needed. Provide back up for Data Coordinator on applicable trials.

Qualifications

• Bachelor’s degree
• Minimum of two years of clinical research or related experience.  Previous experience in oncology research is preferred. 
• This position requires excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment
• Must be a self-starter with the ability to locate resources and operate productively in an environment where standard operating procedures, guidelines and policies are not always available
• Collaborative focus is essential, as are strong written and verbal communication skills, including computer skills
• Must be willing to work a M-F schedule and have the flexibility to manage patients visits that may occur before or after regular work hours
• CCRP or CCRC accreditation preferred

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Clinical Resrearch Coordinator will coordinate day-to-day activities for clinical research protocols for the Pulmonary Critical Care Faculty at Fred Hutch for while demonstrating competence in clinical research skills, problem-solving, and priority setting. The Project Coordinator will participate in the planning, coordination and implementation of complex investigator-initiated clinical research studies involving human subjects, including a multi-year, multi-center observational study of lung disease in cancer patients. This individual will be required to perform their responsibilities with a high level of independence within the scope of study protocol(s) and institutional guidelines, and collaborate with a multi-disciplinary clinical and research team. This individual will report directly to the Investigator in the Pulmonary Section in the Clinical Research Division.

Responsibilities

Study Conduct / Clinical Research Practice:

• Work independently in performing daily responsibilities required to plan and execute clinical research trials and non-intervention protocols.
• Coordinate research and administrative activities related to studies, ensuring all projects are completed according to project timelines.
• Screen, enroll, and follow research subjects, complete case report forms (CRFs), place physician orders, coordinate research study visits, communicate with the primary care teams, and research subjects.
• Meet with Investigator on a regular basis to monitor study data and implement patient communication procedures as per study protocol.
• Interact with research subject to ensure compliance with study procedures involving home monitoring of lung function and sample collection.
• Coordinate specimen collection, transport, processing, storage, and shipment procedures according to protocol requirements. Track and maintain research supplies.
• Serve as a project liaison for 1) home health monitoring company involved in clinical study, 2) secondary sites for project start-up and QI, and 3) other Fred Hutch and Seattle Cancer Care Alliance departments involved in the study.
• On assigned interventional clinical trials, act as the main protocol resource person for the investigator and/or research sponsor, research subjects, local and central labs, monitors, primary care teams, and investigational pharmacy staff.
• Collaborate with investigators and clinical staff to ensure appropriate identification, enrollment, and follow-up of subjects for completion of study activities.
• Train others as needed and develop standard operating procedures (SOP) or other necessary documents for standardized study conduct.
• Ensure accurate enrollment records are maintained and up to date.
• Create source documents or CRFs as needed to promote efficient data collection and entry.
• Review CRFs to ensure completeness, accuracy, and compliance with Good Clinical Practice.
• Identify and report any adverse events in accordance with protocol, regulatory guidelines, and institutional policy.

Protocol Development and Implementation:

• Help review, update, and develop standard operating procedures for research protocols as needed.
• Develop and maintain tools for study implementation, which may include data collection tools, study reference materials, and study specific orders. Revise and utilize tools as necessary to fulfill the aims of the clinical trial.

Regulatory Compliance and Documentation:

• Facilitate protocol monitoring visits and collaborate with study monitors to resolve data discrepancies and procedural issues.
• Provide input to the regulatory coordinator on protocol document submissions and continuing review reports.
• Prepare or assist in preparing consent forms, continuation review reports, protocol modifications, serious adverse event reports, and other study reports.

Other Duties:

• Perform retrospective chart review as required
• Travel for investigator meetings to secondary sites for study start-up
• Other duties as assigned

Qualifications

Required:

• A bachelor's degree is required.  
• Computer experience including electronic CRF, MS Office including Excel, Outlook, PowerPoint and Access.
• Excellent written and communication skills, attention to detail, high-level organization, leadership ability, and the flexibility to work in collaboration with a multi-disciplinary team.

Preferred:

• One-year post-master’s or two years post-bachelor’s project coordination experience in a research setting.
• Agility with smartphone technology and web-based databases is desirable.
• Knowledge using and building REDCap databases is desirable.
• Certified Clinical Research Coordinator (ACRP), Certified Clinical Research Professional (SOCRA), or equivalent certification.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Clinical Research Coordinator I/II (CRC I/II) will coordinate day-to-day activities for assigned clinical research protocols for the Infectious Disease Sciences Program while demonstrating competence in clinical research skills, problem-solving, and priority setting.

Responsibilities

The incumbent will participate in the planning, coordination, and implementation of complex investigator-initiated, industry-sponsored, and cooperative group clinical research studies involving human subjects. This individual will work under the supervision of the Clinical Trial Program Manager and will be required to perform their responsibilities with independence within the scope of study protocol(s) and institutional guidelines. Collaborate with a multi-disciplinary team and provide guidance to other study staff in carrying out research implementation tasks. The incumbent will some or all the following responsibilities:

Study Conduct / Clinical Research Practice

• Work independently in performing daily responsibilities required to plan and execute investigator driven/industry-based clinical research trials and non-intervention protocols.
• Coordinate research and administrative activities related to studies, ensuring all projects are completed according to project timelines.
• Serve as project liaison, representing the project to other center departments, funding sources, affiliated individuals or institutions, and outside organizations.
• On assigned projects, act as the main protocol resource person for the investigator and/or research sponsor, research subjects, local and central labs, monitors, primary care teams, and investigational pharmacy staff.
• Collaborate with investigators and coworkers to ensure completion of study activities
• Train others as needed and develop standard operating procedures (SOP) or other necessary documents for standardized study conduct.
• Screen and recruit subjects either within the consortium or the community dependent upon study specific requirements, enroll, and follow research subjects, complete case report forms (CRFs), place physician orders, coordinate research study visits, communicate with the primary care teams, investigational pharmacy staff and research subjects.
• Travel to University of Medical Center, Seattle Children’s, and Seattle Cancer Care Alliance will be required for the enrollment of study subjects.
• Ensure accurate enrollment records are maintained and up to date.
• Coordinate specimen collection, transport, processing, storage, and shipment procedures according to protocol requirements. Track and maintain research supplies.
• Create source documents or CRFs as needed to promote efficient data collection and entry.
• Review CRFs to ensure completeness, accuracy, and compliance with Good Clinical Practice.
• Identify and report any adverse events in accordance with protocol, regulatory guidelines, and institutional policy.

Protocol Development and Implementation

• Help develop and review research protocols for feasibility and collaborate with study leadership to develop the study budget and implementation plans.
• Develop and maintain tools for study implementation, which may include data collection tools, study reference materials, and study specific orders. Revise and utilize tools as necessary to fulfill the aims of the clinical trial.

Budget and Billing

• Prepare requests for research prices on study activities and coordinate the research billing start-up process.
• Review, reconcile, and approve research study bills. Work closely with the IDS fiscal staff to ensure accurate research billing and reimbursement.

Regulatory Compliance and Documentation

• Facilitate protocol monitoring visits and collaborate with study monitors to resolve data discrepancies and procedural issues.
• Provide input to the regulatory coordinator on protocol document submissions and continuing review reports.
• Prepare or assist in preparing consent forms, continuation review reports, protocol modifications, serious adverse event reports, and other study reports.

Other duties which may be required:

• Perform retrospective chart review as required
• Travel for investigator meetings
• Will require weekends and holiday coverage for clinical studies.
• Other duties as assigned

Qualifications

• Clinical Research Coordinator I Minimum Education/Experience: BS or higher degree required in scientific/medical field. Previous work experience in a clinical research setting required.
• Clinical Research Coordinator II Minimum Education/Experience: Bachelor’s degree in scientific/medical field or equivalent experience/education. Master’s degree in healthcare related field preferred, particularly in the area of epidemiology. Minimum of three years post-master’s or five years post-bachelor’s experience in clinical study/trials coordination or related field.
• Computer experience including electronic CRF, MS Office including Excel, Outlook, PowerPoint and Access.
• Knowledge using REDCap databases is desirable.
• Excellent written and communication skills, attention to detail, high-level organization, leadership ability, and the flexibility to work in collaboration with a multi-disciplinary team.
• Desire Certified Clinical Research Coordinator (ACRP), Certified Clinical Research Professional (SOCRA), or equivalent certification

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The Clinical Research Coordinator II participates in all aspects of clinical research trials except those that require medical expertise or licensure and leads key tasks such accurate record keeping, data collection and management, and correspondence.

Responsibilities

• Provides day-to-day coordination of clinical research studies including screening patients for protocol eligibility, ensuring informed consent has been properly obtained, enrolling subjects, collecting data and communicating with clinic staff.
• Collaborates with clinic providers and staff, ancillary services, and research staff regarding protocol implementation and operations
• Collects and enters data in a timely manner in accordance with the protocol
• Collects and maintains regulatory documents
• Submits reports and documents as required
• Coordinates the study drug management process
• Coordinates research protocol monitoring and auditing visits and takes action to correct problems such as deviation from protocol requirements to ensure research quality
• Participates in the development of department and/or protocol standard operating procedures and tools
• Participates in the startup of a study including things such as budget development, contracting, and protocol implementation

Qualifications

Required:

• Minimum of 2 years of experience in a clinical research setting
• Proficiency with email, spreadsheets, word processing, and databases
• Experience with electronic medical records systems
• Ability to understand and follow multiple complex protocols at multiple sites
• Ability to organize and manage time and tasks independently
• Ability to develop and/or present content to senior leaders and other groups
• Problem solving skills

Preferred:

• Bachelor's degree or 2 years of clinical research experience
• Certified Clinical Research Coordinator (ACRP), Certified Clinical Research Professional (SOCRA), or equivalent certification
• Oncology research experience
• Knowledge of regulations and guidelines for conducting clinical research; for example, good clinical practice (ICH-GCP), Human Subjects Protocol, etc

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Clinical Research Coordinator I/II (CRC I/II) will coordinate day-to-day activities for assigned clinical research protocols for the Infectious Disease Sciences Program while demonstrating competence in clinical research skills, problem-solving, and priority setting

Responsibilities

The incumbent will participate in the planning, coordination, and implementation of complex investigator-initiated, industry-sponsored, and cooperative group clinical research studies involving human subjects. This individual will work under the supervision of the Clinical Trial Program Manager and will be required to perform their responsibilities with independence within the scope of study protocol(s) and institutional guidelines. Collaborate with a multi-disciplinary team and provide guidance to other study staff in carrying out research implementation tasks. The incumbent will some or all the following responsibilities:

Study Conduct / Clinical Research Practice

• Work independently in performing daily responsibilities required to plan and execute investigator driven/industry-based clinical research trials and non-intervention protocols.
• Coordinate research and administrative activities related to studies, ensuring all projects are completed according to project timelines.
• Serve as project liaison, representing the project to other center departments, funding sources, affiliated individuals or institutions, and outside organizations.
• On assigned projects, act as the main protocol resource person for the investigator and/or research sponsor, research subjects, local and central labs, monitors, primary care teams, and investigational pharmacy staff.
• Collaborate with investigators and coworkers to ensure completion of study activities
• Train others as needed and develop standard operating procedures (SOP) or other necessary documents for standardized study conduct.
• Screen and recruit subjects either within the consortium or the community dependent upon study specific requirements, enroll, and follow research subjects, complete case report forms (CRFs), place physician orders, coordinate research study visits, communicate with the primary care teams, investigational pharmacy staff and research subjects.
• Travel to University of Medical Center, Seattle Children’s, and Seattle Cancer Care Alliance will be required for the enrollment of study subjects.
• Ensure accurate enrollment records are maintained and up to date.
• Coordinate specimen collection, transport, processing, storage, and shipment procedures according to protocol requirements. Track and maintain research supplies.
• Create source documents or CRFs as needed to promote efficient data collection and entry.
• Review CRFs to ensure completeness, accuracy, and compliance with Good Clinical Practice.
• Identify and report any adverse events in accordance with protocol, regulatory guidelines, and institutional policy.

Protocol Development and Implementation

• Help develop and review research protocols for feasibility and collaborate with study leadership to develop the study budget and implementation plans.
• Develop and maintain tools for study implementation, which may include data collection tools, study reference materials, and study specific orders. Revise and utilize tools as necessary to fulfill the aims of the clinical trial.

Budget and Billing

• Prepare requests for research prices on study activities and coordinate the research billing start-up process.
• Review, reconcile, and approve research study bills. Work closely with the IDS fiscal staff to ensure accurate research billing and reimbursement.

Regulatory Compliance and Documentation

• Facilitate protocol monitoring visits and collaborate with study monitors to resolve data discrepancies and procedural issues.
• Provide input to the regulatory coordinator on protocol document submissions and continuing review reports.
• Prepare or assist in preparing consent forms, continuation review reports, protocol modifications, serious adverse event reports, and other study reports.

Other duties which may be required:

• Perform retrospective chart review as required
• Travel for investigator meetings
• Will require weekends and holiday coverage for clinical studies.
• Other duties as assigned

Qualifications

• Clinical Research Coordinator I Minimum Education/Experience: BS or higher degree required in scientific/medical field. Previous work experience in a clinical research setting required.
• Clinical Research Coordinator II Minimum Education/Experience: Bachelor’s degree in scientific/medical field or equivalent experience/education. Master’s degree in healthcare related field preferred, particularly in the area of epidemiology. Minimum of three years post-master’s or five years post-bachelor’s experience in clinical study/trials coordination or related field.
• Computer experience including electronic CRF, MS Office including Excel, Outlook, PowerPoint and Access.
• Knowledge using REDCap databases is desirable.
• Excellent written and communication skills, attention to detail, high-level organization, leadership ability, and the flexibility to work in collaboration with a multi-disciplinary team.
• Desire Certified Clinical Research Coordinator (ACRP), Certified Clinical Research Professional (SOCRA), or equivalent certification

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

This individual will work under the supervision of the Principal Investigator(s) and will be required to perform their esponsibilities with a high level of independence within the scope of study protocol(s) and institutional guidelines. The ability to work across Fred Hutchinson, University of Washington and Seattle Cancer Care Alliance will be critical.

The ideal candidate will be able to address the full set of responsibilities in this listing and commit to a 1.0 FTE position.

Responsibilities

• Principal Investigator Support:
  • Serve as designee of the Principal Investigator (PI) to manage the daily clinical operations of assigned research studies in accordance with regulatory, GCP guidelines and institutional policy
  • Liase with SCCA clinical and administrative teams to identify appropriate and effective recruitment pathways

• Recruitment and Enrollment
  • Review study candidates’ medical records for study eligibility
  • Ensure informed consent, initiate patient enrollment, and ensure accurate enrollment records are maintained

• Education
  • Educate clinical teams, co-investigators, ancillary departments, and patients to ensure safe and accurate protocol implementation

• Protocol Implementation
  • Because the nature of the clinical study may vary within this job, the CRC must be capable of moving seamlessly between different protocols
  • Develop and maintain tools for study implementation, which may include data collection tools, study reference materials, and study specific orders. Revise and utilize tools as necessary to fulfill the aims of the clinical trial.
  • Initiate scheduling of patient clinic visits, and on-going study visits. Ensure clinical procedures, lab test, and other protocol specific activities are completed as outlined in the protocols.
  • Complete requisition forms, assemble kits for upcoming research visits, transport laboratory samples, and ensure samples are processed and shipped according to study specific guidelines, while tracking and maintaining research supplies.

• Budget & Billing
  • Understand clinical trial budget and billing plans for patients enrolled on clinical trials or studies
  • Work with internal partners to obtain and submit budget and billing information

• Other Duties Which May Be Required
  • Assist the Principal Investigator (PI) with protocol development, revision, and study analysis
  • Collaborate with Investigational Drug Services (IDS) on drug assignment, dispensation information, and maintain regular communication regarding status of study subjects
  • Ensure study drug self-administration and accountability with patients
  • Perform non-clinical ECGs
  • Administer study questionnaires and disperse study-related payments
  • Conduct study interviews and participate in focus groups
  • Function as a protocol liaison with clinical teams, patients, and when necessary, other institutions or drug companies
  • Maintain or assist in maintaining IRB correspondence and regulatory documentation.  Prepare or assist in preparing consent forms, continuation review reports, protocol submissions and modifications, and other study reports
  • Maintain appropriate source documentation, and complete or assist with accurate data entry into case report forms in a timely manner
  • Coordinate monitoring visits and respond to queries and other requests from study monitors
  • Identify and report adverse events in accordance with protocol, regulatory guidelines, and institutional policy
  • Participate in the review of charges for patients on clinical trials to ensure billing compliance
  • Travel for industry sponsored investigator meetings
  • Maintain knowledge in the field through attending related project meetings, reading related literature, and maintaining professional associations
  • Other duties as assigned

Qualifications

• Associate degree required, with Bachelor’s degree preferred
• Applicant must have a minimum of one to two years of clinical research or related experience.
• Previous experience in biobehavioral intervention studies (e.g. web apps, acupuncture) is preferred
• Previous experience in oncology research and clinical data collection is preferred
• Previous experience in investigator-initiated and industry-sponsored drug studies is preferred
• Previous experience in survey research and qualitative interviewing is preferred
• This position requires excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment
• Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The position will work directly with an Assistant Member in the Infectious Disease Sciences Program in the Vaccine and Infectious Disease Division to provide support to the PI and research staff in the development, implementation and management of his diverse research portfolio, including research studies and clinical trials.

The Clinical Research Coordinator (CRC) will be responsible for providing support on all aspects of research study and clinical trial development and implementation. Primary responsibilities of the CRC will include assistance with the planning, coordination, implementation, and close-out (e.g. presentation of data, manuscript writing) of industry-sponsored clinical trials, in addition to retrospective and prospective observational or investigator-initiated interventional studies. Additional responsibilities will include communicating with internal and external collaborators and supporting study personnel in the preparation of regulatory documentation and audits if applicable.

Under the supervision of the Research Manager and the PI, the CRC will manage a portfolio of clinical research projects and will be required to perform their responsibilities with a high level of independence within the scope of study protocol(s) and institutional guidelines. The position will include interaction with patients, physicians, researchers, and other clinical providers and support staff within and outside of the Fred Hutch/ Seattle Cancer Care Alliance (SCCA) / UW system including the SCCA Patient Care Services.

Responsibilities

• Assist the research manager with preparing start-up documentation including IRB documents, eligibility checklists, study procedures/SOPs, study-specific clinic orders and study calendars (if not completed by the Clinical Research Manager)
• Screens and registers patients; ensures eligibility requirements are met
• Ability to consent patients and assures consent forms are completed correctly and in entirety
• Schedules study related clinic procedures such as blood draws, infusions and imaging according to protocol requirements; coordinates with clinic staff to ensure proper documentation and timing of research-related procedures
• Perform review of medical charts using ORCA/MINDscape and enter data in REDCap, Excel or other study-related databases
• Abstracts data from medical records to complete study-specific case-report form (CRFs) (electronic and/or paper) in timely and accurate manner; maintains shadow chart with source documents
• Maintain study and specimen tracking and inventory records for biospecimens pulled from repository.
• Assemble study kits for clinical trials.
• Perform basic processing and banking of lab specimens and associated record keeping
• Collaborates with study sponsor/consortium delegate to assist with study monitoring visits and responds to findings
• Creates and maintains patient tracking tools; communicates status to investigators, management and relevant departments
• Manages study documentation throughout study life cycle including IRB annual renewals, modifications, patient study charts and regulatory binder
• Liaises with study sponsor, investigator(s), research manager and members of study team to communicate timelines, expectations and study status
• Acts as a resource to physicians, investigators, other staff members, and other organizations regarding protocol procedures, data collection requirements and other study related operations
• Keeps knowledge and skills current by completing mandated training and attending meetings with the study team and the Consortium, such as the monthly coordinator meeting, relevant lectures, faculty and administrative presentations, and other opportunities of interest
• Perform other duties as assigned.

Qualifications

Clinical Research Coordinator II Minimum Education/Experience

Bachelor’s degree in scientific/medical field or equivalent experience/education. Master’s degree in healthcare related field is preferred. Minimum of three years post-master’s or five years post-bachelor’s experience in clinical study/trials coordination or related field.

• Clinical research related certification is preferred.
• Experience with industry-sponsored clinical trials and documentation of case report form (eCRF) in study electronic data capture (EDC) system
• Ability to work in teams and independently, flexible hours at times in support of clinical trials and regulatory and related compliance
• Strong attention to detail and project management skills and experience is required
• Well-organized and ability to juggle numerous tasks, often with conflicting and competing deadlines
• Strong written and verbal communication skills
• Strong computer skills, including proficiency in the Office Suite, and experience working with excel and databases (preferably REDCap)
• Knowledge of federal regulations and guidelines that govern clinical research, including GCP and human subjects research       

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Clinical Research Coordinator (CRC), Immunotherapy is responsible for day-to-day coordination of intervention Phase I-III clinical trials. The position will perform all tasks relating to the start-up, management and close-out of studies including: preparing IRB documentation, maintaining study records, screening patients for eligibility, tracking patient visits, and abstracting and reporting data. The Coordinator will work on multiple studies for one or more investigators, and report regularly to those investigators on the progress of the studies. The CRC II reports directly to the Clinical Research Manager.

Responsibilities

• Prepares study start-up documentation including IRB documents, eligibility checklists, study-specific clinic orders and study calendars (if not completed by the Clinical Research Manager)
• Screens and registers patients; ensures eligibility requirements are met
• Assures consent forms are completed correctly and in entirety
• Schedules study related clinic procedures such as blood draws, infusions and imaging according to protocol requirements; coordinates with clinic staff to ensure proper documentation and timing of research-related procedures
• Abstracts data from medical records to complete study-specific CRFs (electronic and/or paper) in timely and accurate manner; maintains shadow chart with source documents
• Collaborates with study sponsor/consortium delegate to assist with study monitoring visits and responds to findings
• Creates and maintains patient tracking tools; communicates status to investigators, management and relevant departments
• Manages study documentation throughout study life cycle including IRB annual renewals, modifications, patient study charts and regulatory binder
• Liaises with study sponsor, investigator(s) and members of study team to communicate timelines, expectations and study status
• Acts as a resource to physicians, investigators, other staff members, and other organizations regarding protocol procedures, data collection requirements and other study related operations
• Keeps knowledge and skills current by completing mandated training and attending meetings with the study team and the Consortium, such as the monthly coordinator meeting, relevant brown bags, faculty and administrative presentations, and other opportunities of interest

Qualifications

• 2 -3 years’ experience in trial coordination and management is critical to success in this position, given volume, complexity, and compliance requirements in support of clinical trials
• Undergraduate degree is mandatory, with master's degree preferable and/or equivalent experience at that level
• Ability to work in teams and independently, flexible hours at times in support of clinical trials and regulatory and related compliance
• Ability to work with faculty and staff, including clinicians, and research scientists
• Attention to detail and project management skills and experience
• Well-organized and ability to juggle numerous tasks, often with conflicting and competing deadlines
• Experience with study Data systems (Medidata RAVE, etc.) is strongly preferred

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Clinical Research Nurse will work collaboratively with a multidisciplinary team in the implementation, conduct and evaluation of clinical research studies involving novel cellular immunotherapies for cancer patients. This individual will work under the supervision of The Clinical Research Operations Manager in the Integrated Immunotherapy Research Center Clinical Operations Program.

The Clinical Research Nurse performs their responsibilities with in their scope of practice with a high level of independence under the authority of attending physicians. The incumbent works collaboratively with other team members to manage the daily clinical operations of assigned research studies in accordance with regulatory and GCP guidelines and institutional policy.

Responsibilities

• Develop tools for study implementation including eligibility checklist, study reference materials, standing orders and clinical summaries.
• Determine patient study eligibility, ensure informed consent, and monitor patient’s clinical course
• Perform clinical procedures including blood draws, vital signs, drug administration, and specimen collection as outlined in the protocols.
• Act as a clinical liaison for protocols with clinical teams, patients, other institutions, and drug companies.
• Educate clinical teams, ancillary departments, patients, and families about protocols to ensure safe and accurate implementation in compliance with protocol requirements.
• Assist in maintaining IRB and FDA correspondence and regulatory documentation related to patient care and adverse events
• Assist in preparing continuation review reports, protocol modifications, and other study reports.
• Maintain appropriate source documentation, and complete case report forms. Compile and present status reports to PI, research team, sponsors, nursing staff, and physicians.
• Identify, assess, and report adverse events in accordance with protocol and regulatory guidelines, and institutional policy.
• Provide guidance and mentorship to support staff in the execution of their duties relative to protocol coordination.
• Maintain thorough knowledge in the field through attending related project meetings and symposia, reading related literature, and maintaining professional associations.

Qualifications

• Active Registered Nurse license in the state of Washington required.
• Current Basic Life Support Healthcare Provider Card from American Heart Association
• A minimum of two years of nursing experience.
• Previous experience in oncology and research is strongly preferred.
• Strong written and verbal communication skills including computer skills are essential.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Clinical Research Nurse will work collaboratively with a multidisciplinary team in the implementation, conduct and evaluation of clinical research studies involving novel cellular immunotherapies for cancer patients. This individual will work under the supervision of The Clinical Research Operations Manager in the Integrated Immunotherapy Research Center Clinical Operations Program.

The Clinical Research Nurse performs their responsibilities with in their scope of practice with a high level of independence under the authority of attending physicians. The incumbent works collaboratively with other team members to manage the daily clinical operations of assigned research studies in accordance with regulatory and GCP guidelines and institutional policy.

Responsibilities

• Develop tools for study implementation including eligibility checklist, study reference materials, standing orders and clinical summaries.
• Determine patient study eligibility, ensure informed consent, and monitor patient’s clinical course
• Perform clinical procedures including blood draws, vital signs, drug administration, and specimen collection as outlined in the protocols.
• Act as a clinical liaison for protocols with clinical teams, patients, other institutions, and drug companies.
• Educate clinical teams, ancillary departments, patients, and families about protocols to ensure safe and accurate implementation in compliance with protocol requirements.
• Assist in maintaining IRB and FDA correspondence and regulatory documentation related to patient care and adverse events
• Assist in preparing continuation review reports, protocol modifications, and other study reports.
• Maintain appropriate source documentation, and complete case report forms. Compile and present status reports to PI, research team, sponsors, nursing staff, and physicians.
• Identify, assess, and report adverse events in accordance with protocol and regulatory guidelines, and institutional policy.
• Provide guidance and mentorship to support staff in the execution of their duties relative to protocol coordination.
• Maintain thorough knowledge in the field through attending related project meetings and symposia, reading related literature, and maintaining professional associations.

Qualifications

• Active Registered Nurse license in the state of Washington required.
• Current Basic Life Support Healthcare Provider Card from American Heart Association
• A minimum of two years of nursing experience.
• Previous experience in oncology and research is strongly preferred.
• Strong written and verbal communication skills including computer skills are essential.

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The Clinical Technologist I performs lab tests and processes on patient samples, which involves operating analytical instruments, compiling and verifying the accuracy of clinical data and complying with the Laboratory QA/QC program. This position is for work in the Pharmacokinetics Lab. This is an extraordinary opportunity to lead continuous disruptive innovations in the fight against cancer.

Schedule: Tuesday - Saturday; 8am-5pm

Responsibilities

• Handles biological specimens and products; performs clinical assays and lab processes by following the Standard Operating Procedures
• Operates analytical instruments, compiles and analyzes clinical data, verifies its accuracy and reports results
• Performs laboratory quality controls measurements
• Prepares reagents and materials for clinical procedures
• Enters patient and specimen information and results into the Laboratory Information Management System (LIMS)
• Performs regular maintenance and troubleshooting on analytical instruments

Qualifications

Required:

• A Bachelor's degree in a chemical, physical, biological or clinical laboratory science, or medical technology from an accredited institution OR an associate degree in a laboratory science or medical laboratory technology from an accredited institution or equivalent education and training that includes 24 semester hours of science courses that includes six semester hours of chemistry, six semester hours of biology and twelve semester hours of chemistry, biology or medical laboratory technology in any combination AND have laboratory training that includes completion of a clinical laboratory training program approved or accredited by an HHS-approved organization, or at least 3 months documented laboratory training in each specialty in which the individual performs high complexity testing
• Must obtain ASCP certification within 15 months of hire
• Proficiency with email, spreadsheets, and word processing
• Manual computation skills
• Ability to communicate verbally in person, on the phone, and in writing in a clear, concise and professional manner
• Attention to detail
• Ability to work in a high pressure, time-sensitive, and complex health care environment
• Ability to identify and triage issues appropriately
• Familiarity with medical terminology

Preferred:

• One year of clinical lab or research
• ASCP or equivalent certification is preferred
• Medical Laboratory Scientist, Medical Technologist or an equivalent certification
• Gas Chromatography or liquid chromatography experience

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The Clinical Technologist I perform lab tests and processes on patient samples or products which involves operating analytical instruments, compiling and verifying the accuracy of clinical data and complying with the Laboratory QA/QC program. This position is for a generalist Medical Laboratory Scientist for work in both Chemistry and Hematology departments in the Alliance Lab.

Responsibilities

• Handles biological specimens and products; performs clinical assays and lab processes by following the Standard Operating Procedures
• Operates analytical instruments, compiles and analyzes clinical data, verifies its accuracy and reports results
• Performs laboratory quality controls measurements
• Prepares reagents and materials for clinical procedures
• Enters patient and specimen information and results into the Laboratory Information Management System (LIMS)
• Performs regular maintenance and troubleshooting on analytical instruments

Qualifications

Required:

• A Bachelor’s degree in a chemical, physical, biological or clinical laboratory science, or medical technology from an accredited institution OR An associate degree in a laboratory science or medical laboratory technology from an accredited institution or equivalent education and training that includes 24 semester hours of medical laboratory technology courses or 24 semester hours of science courses that include six semester hours of chemistry, six semester hours of biology and twelve semester hours of chemistry, biology, or medical laboratory technology in any combination AND have laboratory training that includes completion of a clinical laboratory training program approved or accredited by an HHS-approved organization, or at least 3 months documented laboratory training is each specialty in which the individual performs high complexity testing.
• Medical Laboratory Scientist, Medical Technologist or an equivalent certification through ASCP or AMT
• Proficiency with email, spreadsheets, and word processing
• Manual computation skills
• Ability to communicate verbally in person, on the phone, and in writing in a clear, concise and professional manner
• Attention to detail
• Ability to work in a high pressure, time-sensitive, and complex health care environment
• Ability to identify and triage issues appropriately
• Familiarity with medical terminology

Preferred:

• One year of clinical lab or research experience

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The Clinical Technologist I performs lab tests and processes on patient samples or products which involves operating analytical instruments, compiling and verifying the accuracy of clinical data and complying with the Laboratory QA/QC program. This position is for a generalist Medical Laboratory Scientist for work in both Chemistry and Hematology departments in the Alliance Lab.

Work Schedule: M-F; 10:00 AM-6:30 PM

Responsibilities

• Handles biological specimens and products; performs clinical assays and lab processes by following the Standard Operating Procedures.
• Operates analytical instruments, compiles and analyzes clinical data, verifies its accuracy and reports results
• Performs laboratory quality controls measurements
• Prepares reagents and materials for clinical procedures
• Enters patient and specimen information and results into the Laboratory Information Management System (LIMS)
• Performs regular maintenance and troubleshooting on analytical instruments

Qualifications

• A Bachelor’s degree in a chemical, physical, biological or clinical laboratory science, or medical technology from an accredited institution OR An associate degree in a laboratory science or medical laboratory technology from an accredited institution or equivalent education and training that includes 24 semester hours of medical laboratory technology courses or 24 semester hours of science courses that include six semester hours of chemistry, six semester hours of biology and twelve semester hours of chemistry, biology, or medical laboratory technology in any combination AND have laboratory training that includes completion of a clinical laboratory training program approved or accredited by an HHS-approved organization, or at least 3 months documented laboratory training is each specialty in which the individual performs high complexity testing.
• Medical Laboratory Scientist, Medical Technologist or an equivalent certification through ASCP or AMT
• Proficiency with email, spreadsheets, and word processing
• Manual computation skills
• Ability to communicate verbally in person, on the phone, and in writing in a clear, concise and professional manner
• Attention to detail
• Ability to work in a high pressure, time-sensitive, and complex health care environment
• Ability to identify and triage issues appropriately
• Familiarity with medical terminology
• One year of clinical lab or research preferred

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The Clinical Technologist I, certified performs lab tests, and processes on patient samples or products which involves operating analytical instruments, compiling and verifying the accuracy of clinical data and complying with the laboratory QA/QC program. This position is for a generalist Medical Laboratory Scientist for work in both Chemistry and Hematology departments in the Alliance Lab.

Work Schedule: M-F; 0800 – 1630

Responsibilities

• Handles biological specimens and products; performs clinical assays and lab processes by following the Standard Operating Procedures.
• Operates analytical instruments, compiles and analyzes clinical data, verifies its accuracy and reports results
• Performs laboratory quality controls measurements
• Prepares reagents and materials for clinical procedures
• Enters patient and specimen information and results into the Laboratory Information Management System (LIMS)
• Performs regular maintenance and troubleshooting on analytical instruments

Qualifications

• A Bachelor’s degree in a chemical, physical, biological or clinical laboratory science, or medical technology from an accredited institution OR an associate degree in a laboratory science or medical laboratory technology from an accredited institution or equivalent education and training that includes 24 semester hours of medical laboratory technology courses or 24 semester hours of science courses that include six semester hours of chemistry, six semester hours of biology and twelve semester hours of chemistry, biology, or medical laboratory technology in any combination AND have laboratory training that includes completion of a clinical laboratory training program approved or accredited by an HHS-approved organization, or at least 3 months documented laboratory training is each specialty in which the individual performs high complexity testing
• ASCP or equivalent certification is required
• Proficiency with email, spreadsheets, and word processing
• Manual computation skills
• Ability to communicate verbally in person, on the phone, and in writing in a clear, concise and professional manner
• Attention to detail
• Ability to work in a high pressure, time-sensitive, and complex health care environment
• Ability to identify and triage issues appropriately
• Familiarity with medical terminology
• One year of clinical lab or research preferred

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The Coding Specialist complies with the Official Coding Guidelines in ICD-10-CM and CPT coding conventions to assign for diagnoses and procedure codes for SCCA’s outpatient facility services. Clinical judgment and high level analytical skills are utilized to code and abstract the legal medical record to support appropriate reimbursement, physician documentation improvement, clinical effectiveness, outcome studies, and research to meet regulatory accreditation requirements for state and federal reporting and other external reporting purposes. This position offers a combination of remote and on-site coding but it is not a full-time remote position.

Responsibilities

• Understand and apply correct coding, regulatory and compliance guidelines, APCs, ICD10, CPT, E&M, procedure codes and modifiers, and applies documentation guidelines
• Maintains 95% coding accuracy while meeting department's productivity standards
• Participate in staff discussions and provides valuable input to the team

Qualifications

Required:

• High School Degree, GED, or equivalent combination of education and experience from which comparable knowledge and abilities can be acquired is necessary
• RHIA, RHIT, CCS, CPC, COC, CCS-P
• A minimum of 2 years experience in outpatient facility abstracting coding (ICD9,ICD10, HCPCS and CPT) and facility coding modifiers. Experience may be substituted for a Bachelor's degree in Health Informatics or Health Information Management along with required certification.
• Working knowledge of insurance plans, LCD/NCD’s
• Ability to work with clinical professionals
• Medical records and EMR/EHR knowledge
• Medical terminology, Anatomy and Physiology

Preferred:

• Bachelor’s degree
• Prior oncology or Transplant coding
• Prior training experience with clinicians
• E & M, Surgical and Infusion coding
• ICD10 training and/or Dual/Double coding experience
• EPIC HB, 3M encoder ORCA and Mindscape experience

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Committee Operations Manager will be responsible for overseeing the Cancer Consortium’s clinical trial oversight committees, including the Scientific Review Committees (SRCs) and the central Data and Safety Monitoring Committee (DSMC) and individual study Data and Safety Monitoring Boards (DSMBs). The position is responsible for ensuring that these functions meet all federal and institutional requirements and that the operations are supported by sufficient documentation and staffing resources. The position will work closely with Consortium faculty and leadership to provide performance metrics and to report overall committee performance. This position requires understanding the clinical research process and the NCI’s cancer center requirements for scientific review. The position reports directly to the Sr. Operations Manager and supervises 1-2 Committee Coordinators.

Responsibilities

• Manage the Consortium’s SRCs and DSMC, ensuring that the committees meet all NCI and Consortium review requirements.
• Ensure committees have:
  • Appropriate faculty membership and Chair oversight
  • New committee membership training
  • Sufficient meeting and review documentation
  • Review times that meet defined turn-around-time standards
  • Liaise with the Consortium’s Institutional Review Office to ensure appropriate committee communication between the SRC and IRB.
  • In collaboration with committee chairs, manage membership rosters
  • Collate and present quarterly SRC metrics including review timelines, approval rates, low trial accrual review closures; recommend operational changes to correct any issues
• Manage the Consortium low-accrual policy and propose any changes to ensure accruals meet NCI requirements
• Develop and maintain standard operating procedures, reviewer forms, and meeting templates for committee management
• Define, track and generate regular performance metrics for committees
• Plan and manage resources to support all applicable committee functions; plan for increased DSMB management
• Liaise with Clinical Trial Management System (CTMS) Program Office to ensure required data is captured and QCd to meet committee management and reporting needs
• Identify and implement technical solutions to support efficient committee operations; define system requirements and create user support documentation

Qualifications

Experience and Abilities

• 3-5 years managing clinical research operations, preferably in oncology
• Managing faculty committees
• Working with multi-disciplinary teams
• Managing research data sets
• Communicating with all levels of a research organization

Knowledge and Skills

• Bachelor’s Degree
• Clinical research related certification preferred
• Strong verbal and written communication skills
• Knowledge of applicable local, state and federal regulations and guidelines
• Understanding of NCI Cancer Center clinical trial infrastructure

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Office of Community Outreach and Engagement (OCOE) for the Fred Hutch/University of Washington Cancer Consortium (the Consortium) is seeking a leader and team player for the role of Community Health Education (CHE) Manager. The CHE Manager will oversee outreach and engagement work in support of the OCOE strategic plan. This role will report to the OCOE Program Administrator.

The CHE Manager will facilitate partnerships among Consortium researchers, OCOE staff, and external organizations on collaborative projects related to health equity in the Consortium’s 13-county catchment area. The CHE Manager will manage 4 Community Health Educators (CHEs), supporting and supervising them as they conduct outreach, education, and research with communities that are disproportionately represented in cancer incidence and mortality, including American Indian/Alaskan Native, African Americans/Black, Asian American, Hispanic/Latinx, those living in rural areas, those with low socio-economic status, uninsured/underinsured, and other disenfranchised individuals.

Responsibilities

The CHE Manager will work independently in performing daily responsibilities of supervising, coordinating, and overseeing the 4 CHEs in the OCOE. Special skills and knowledge are applied in directing the CHEs to cover the entire catchment area and ensure that the community voice is heard and brought to the OCOE on a regular and continuing basis. Annually, the CHE Manager will oversee the implementation of a catchment area needs assessment that will provide information to the Community Action Coalition about the state of cancer incidence and mortality in the catchment area. They will prepare an annual summary report of the needs assessment. Activities include preparing, facilitating and coordinating individuals and groups to support the OCOE in its outreach to the catchment area. The CHE Manager will be responsible for writing reports to the community, the Internal Advisory Committee, the Consortium, and to the National Institutes of Health.

The CHE Manager will perform some or all of the following responsibilities:

• Oversee four CHEs
• Develop materials and products based on principles and methods of health education and promotion
• Demonstrate strong verbal and written communication skills with established strong writing of health communications, media materials, and presentations
• Develop and implement policies and procedures according to protocol, IRB, grant/contract and Center specifications
• Develop curriculum and training materials with CHEs and community members
• Practice community-based participatory research in community engagement and interaction; coordinate with community organizations
• Collaborate with other Consortium entities, such as University of Washington and Seattle Cancer Care Alliance programs
• Oversee the development of public health interventions consistent with the OCOE strategic plan and annual action plans produced by the OCOE Team in partnership with the Community Action Coalition
• Coordinate the activities of multiple stakeholders as they implement the activities identified by the Community Action Coalition
• Coordinate meetings and events
• Coordinate timely completion and submission of HR documents, expense reimbursement, and credit card reconciliation
• Practice and knowledge of cultural sensitivity with diverse populations in the Cancer Consortium catchment area
• Manage OCOE pilot grants and small grants, including overseeing grantees, and monitoring IRB
• Facilitate weekly staff meetings
• Ensure that project information is presented at regional and national conferences
• Monitor OCOE web pages, SharePoint, social media accounts (Facebook, Twitter, etc.)
• Coordinate CHE training and development
• Travel within the catchment area for events and meetings with the partner organizations
• Other duties as assigned

Qualifications

Required:

• Bachelor’s degree in related field required with at least 5 years of post-bachelor’s relevant experience and training
• Requires excellent written skills
• Outstanding interpersonal, customer service and verbal communication skills
• Must have demonstrated cultural humility
• Demonstrated excellent human relations, facilitation and influencing skills to deal effectively with a broad range of people
• Ability to manage relationships effectively and build collaborative bridges
• Experience supervising multiple staff
• Excellent leadership and organizational management skills
• Experience managing multiple projects from inception to completion
• Ability to think critically and synthesize complex issues to move project forward
• Demonstrated ability to work independently
• Professional experience in public health
• Strong computer skills, including database creation and management (e.g., EndNote, REDCap, Access) and strong knowledge of Microsoft Office software.
• Must be flexible and willing to work occasional evenings and weekends.

Preferred:

• Master’s degree in related field with at least 2 years of post-master’s relevant experience
• Experience working in an academic or scientific research environment

Professional attributes:

• Problem solver
• Detail-oriented
• Maintain a high level of confidentiality, sound judgment
• Motivated by challenge to solve problems and positively affect systems and people
• Positive attitude and sense of humor

Fred Hutchinson Cancer Research Center invites applications for an open faculty position in the Division of Basic Sciences. Recruitment at an Assistant Member level is preferred but we will consider more senior applicants. We seek an exceptional structural biologist conducting fundamental research within areas of molecular and cellular biology that possess significant potential for novel biological insight and discovery. A particularly strong expertise and focus on the use of Cryo-electron microscopy (CryoEM) as their primary experimental approach is required.

Fred Hutch provides outstanding colleagues, a collegial atmosphere, and a wealth of resources to support junior faculty success. Graduate students are drawn from the outstanding ‘Molecular and Cellular Biology’ and ‘Biophysics, Structure and Design’ graduate programs at the University of Washington. Fred Hutch is located in a modern campus by Lake Union in Seattle, Washington, and is close to other non-profit research institutes and the University of Washington. See our website for further information (www.fredhutch.org/basic/).

For consideration, applicants must have a doctoral degree and a substantial record of achievement pre and post-doctoral. Applicants from underrepresented populations are particularly encouraged to apply. Application deadline for consideration for a fall interview: August 31, 2019. Applications will be considered on a rolling basis after the deadline if the position is not filled. Candidates should visit http://apply.interfolio.com/64580 for application instructions.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

Responsibilities

This person will serve in a full-time role of data analyst/programmer, working under the direct mentorship of the group lead data analyst. The engineer will be focused on: 

• building expertise on the internal clinical research dataset and data systems.
• understanding and supporting the different business functions that our systems coordinate, both for research users on the Fred Hutch side and clinical users engaged in patient care and clinical operations.
• working with scientific researchers to analyze and understand clinical data;
• supporting clinical operations of SCCA and Fred Hutch (including system data interfaces with external institutions of the Consortium);
• programming and automating reports to extract and deliver clinical data to investigators, clinicians and clinical support staff; and
• providing research application of our clinical data integrated with external data sources (Amalga) on behalf of CRD’s scientific mission.

Qualifications

Required:

• Bachelor’s degree
• Minimum of 3-6 years (ASE II), or 6-9 years (ASE III) of directly related experience
• Experience in working with Microsoft SQL Server and related Microsoft products
• Strong skills in analyzing relational data and problem solving
• Excellent verbal and written communication skills

Preferred:

• Experience in working in the health care and/or medical research fields
• Experience with HL7 intersystem data interface engines

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

Working under supervision, the Data Analyst II will utilize a preapproved business intelligence tool or direct SQL development to create reporting artifacts including but not limited to: simple reports, complex reports , dashboards , cubes , data visualizations and data mining constructs in support of Fred Hutch and the organizational goals of various consortium partners.

Responsibilities

• Gathering and documenting requirements from the user community and then translating those requirements into an analytics solution that meets the customer’s needs
• Produce high-quality output consistent with team and industry best practices
• Acquire knowledge of preapproved business intelligence tool set functionality and options
• Possess knowledge on a wide range of possible reporting solutions and have sufficient discernment skills to select the most appropriate solution for each set of requirements
• Have an in-depth understanding of the SQL programming language
• Will serve as a liaison with the business community around the usage and deployment of reporting solutions and tools
• Will participate/lead code review sessions and will be expected to make updates as directed by the primary reviewer
• Will have an understanding of reporting within both a relational and a dimensional framework
• Respond to ad hoc requests for reports and other artifacts
• Participate in change control, problem management, and communication process
• Utilizing approved BI tools translate written requirement documents into appropriate reporting artifacts
• Prepare for and actively participate in design and development reviews
• Strictly adhere to established reporting guidelines and standards
• Assist in preparing work estimates for assigned projects
• Meet required deadlines as outlined by project team and business partners
• Prepare documentation for deployment purposes and respond to any implementation issues as needed to ensure quality deliverable has been met
• Assist the data quality team in tracking down/debugging potential data quality issues

Qualifications

Minimum qualifications

• BS in Computer Science, Engineering or equivalent experience
• Minimum of 3 years professional database reporting development experience with a wide range of business intelligence tools (MS Reporting Services, Cognos, Business Objects, Tableau Software, etc.)
• Minimum of 3 years SQL development experience
• Experience working with both relational and dimensional models
• Experience developing a variety of different reporting artifacts (parameterized reports, cubes, dashboards, etc.)
• Sharp analytical abilities, proven design skills and problem solving skills
• Enjoys working in a team environment and has a proven record of positive contributions to the work of the team
• Coordination and working knowledge of project management methodologies (Agile/Scrum), time estimates and allocation

Preferred qualifications

• Experience with Microsoft SQL Server
• Experience gathering and documenting requirements
• some past experience with analytical, data management & reporting tools
• Expertise and knowledge of gathering and documenting analytic/reporting requirements
• Previous work with hospital information systems either connected, or not, to research uses of the data
• Previous experience in delivering to end users reports and/or extracts to support research and/or clinical care

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

Responsibilities

• Abstract clinical research data from patient medical charts
• Code, edit and generally prepare the information according to the CIBMTR standards
• Key enter data into online Web based application, or record on specific data forms for submission to CIBMTR
• Keep up to date with changing forms and procedures
• Assist with data queries as requested. Perform other duties as requested by supervisor
• This position may work with the Immunotherapy Department to coordinate data collection and submission into REDCap database
• Additional training as needed, including HIPAA Training, confidentiality training, human subjects training

Qualifications

• BS or equivalent 5 years experience in related field
• Previous CIBMTR experience preferred
• Must be able to meet required reporting deadlines
• Knowledge of medical records and strong medical terminology a must
• EPIC and Cerner knowledge

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

Biostatistics, Bioinformatics and Epidemiology (BBE) at Fred Hutch is seeking an experienced Data Scientist to work on multiple projects investigating the immunological correlates of vaccine protection for novel tuberculosis and HIV vaccine candidates. The immune response to a vaccine can be highly variable across individuals, particularly for new vaccines that are in active development. Understanding the factors that impact vaccine response and identifying the features of the immune response that confer protection can provide critical feedback for vaccine refinement. As part of the HIV Vaccine Trials Network supported by the NIH Division of AIDS and the Global Health Vaccine Accelerator Program, supported by the Bill and Melinda Gates Foundation we are leading major computational efforts to integrate immunological datasets generated from human vaccine trials. Analysis datasets include those generated by multicolor flow cytometry, transcriptomics/RNAseq, T cell receptor repertoire sequencing, mass spectrometry, microbiome 16S and metagenomic sequencing, and multiplexed systems serology among others.

Responsibilities

The Data Scientist works closely with the PI, a computational biologist and biostatistician, and a growing team, to develop data pipelines, plan and conduct analyses, design and implement data visualizations, and help prepare figures for funding proposals and publication. The ideal candidate should have an appetite to understand and analyze new types of data. 

Qualifications

• M.A., M.S. in computational biology, biostatistics, computer science, data science, bioinformatics or a related field. Candidates with Ph.D. also encouraged to apply.
• 2 - 4 years of hands-on biological data science experience
• Proficiency in Python and/or R programming, with knowledge of the appropriate tools and libraries for working with biological data
• Demonstrated rigor and reproducibility through well organized and well documented code and/or committed to a public code repository (e.g. github)
• Experience analyzing next-generation sequencing data (e.g. transcriptomics, or immune repertoire)
• Preference for candidates having familiarity with dimensionality reduction, regression models, machine learning and/or cloud infrastructure for scalable scientific computing
• Outstanding organizational skills, attention to detail and effective communication are essential
• Eagerness to learn about immunology, vaccines, microbial ecology, biostatistics or whatever the science demands

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Innovation Laboratory (iLab) at Fred Hutch is seeking a Masters- or PhD-level data scientist. The iLab is a new collaborative initiative of the Immunotherapy and Translational Data Science Integrated Research Centers (IIRC and TDS_IRC) with a mission to advance the introduction and development of new immuno-oncology research technologies. The iLab will spur in-house development and early adoption of novel techniques, including advanced single cell RNA spatial sequencing, T- and B-cell receptor sequencing, and other DNA/RNA-based technologies. The data scientist will work closely with lab personnel and immunotherapy researchers to develop data analysis methods for new technologies.

Over the past three years, Fred Hutch has launched three Integrated Research Centers (IRCs) to increase collaborative research across the Center and stimulate transformative cancer discovery. The IIRC, led by Dr. Stanley Riddell, and the TDS_IRC, led by Dr. Raphael Gottardo, have joined together and created the iLab to speed adoption of novel technologies, particularly those that generate large datasets of high utility to immunotherapy. The successful candidate will be embedded in the iLab, but will also have close ties to the Gottardo Lab and the TDS_IRC. The iLab will initially be housed in the Bielas Lab. Working closely with Drs. Bielas and Gottardo, the successful candidate will function with a high degree of independence as they manage daily activities. We see the integration of computational work within the iLab as an integral part of its success, providing computational innovation.

As a Fred Hutch strategic initiative, we value inclusion and a diversity of backgrounds and perspectives to inform our work. We believe in supporting each other through mentorship and providing resources for professional development. Given these values, we strive to make our recruitment and promotion processes fair and transparent. Therefore, we strongly encourage all individuals with an interest in the position to apply. To learn more about the IRCs: Immunotherapy ; Translational Data Science

We are seeking a Masters- or PhD-level data scientist to work with the iLab to develop workflows and data analysis pipelines, from novel genomics technologies developed in-house to collaboration with select industry partners. The data scientist may also support some projects more broadly, creating workflows and analyses that also include data sets generated outside of the iLab, clinical data, and other translation data sources. The ideal candidate will support large collaborative projects in a wide range of problems in oncology research and serve as a consultant/link between the iLab, laboratory and clinical scientists. The incumbent will collaborate with laboratory-based scientists, clinical investigators, biostatisticians, data scientists, programmers and computational biologists in two ways:

• As member of the iLab, creating novel workflows and data analysis pipelines for novel technologies being tested and developed in the laboratory.
• As a contributing member on teams using novel technologies in the iLab, creating and using computational tools for analyzing clinical and pre-clinical samples.

Through these multi-disciplinary collaborations, the data scientist will support and expand opportunities to apply novel tools and technologies to innovative pre-clinical and clinical studies.

Responsibilities

• Consult with Fred Hutch researchers collaborating with iLab to solve their data science problems
• Manage and set scientific priorities across projects
• Develop and optimize computational pipelines to enable the integration and management of large and complex data sets generated in the iLab
• Test and potentially develop open-source software for reproducible research
• Interpret results from computational and statistical analysis
• Assist with study design and analysis of pre-clinical and clinical trials
• Participate in the dissemination of research findings
• Co-author manuscripts for publication

Qualifications

Data Scientist I - Bachelor's degree in bioinformatics, computational biology, biostatistics, statistics, computer science, or a related field and a minimum of 2+ years of hands-on data science experience

Data Scientist II - Bachelor's degree (Master's or PhD preferred) in bioinformatics, computational biology, biostatistics, statistics, computer science, or a related field and a minimum of 5+ years of hands-on data science experience

Data Scientist III - Bachelor's degree (Master's or PhD preferred) in bioinformatics, computational biology, biostatistics, statistics, computer science, or a related field and a minimum of 8+ years of hands-on data science experience

Minimum qualifications (all levels):

• Experience in analysis of next generation sequencing (NGS) data
• Excellent programming skills (Python, R, C/C++, Java) including best software development practices (e.g. design, unit tests, documentation, code review)
• Excellent interpersonal, oral and written communication skills
• Strong work ethic
• Ability to work in a team
• Ability to manage multiple projects and to meet deadlines

Preferred qualifications:

• Experience in high-dimensional data, particularly with NGS and single-cell NGS (e.g. scRNA-seq)
• Experience in cloud computing (e.g. AWS)
• Experience in immunology

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

We’re looking for a Full Stack developer who will take a key role on our team. Our Full Stack developer must have knowledge in all stages of software development. You’ll be working alongside other engineers and developers, collaborating on the various layers of the infrastructure for our web applications that support our patients at Seattle Cancer Care Alliance.

Responsibilities

• Design overall architecture of the web application.
• Maintain quality and ensure responsiveness of applications.
• Collaborate with the rest of the engineering team to design and launch new features.
• Maintain code integrity and organization.
• Experience working with graphic designers and converting designs to visual elements.
• Understanding and implementation of security and data protection.
• Highly experienced with back-end programming languages: Python, JavaScript, Java
• Proficient experience using ReactJS, AWS, SQL
• Familiarity with serverless architecture or SOA
• Experience with Docker and GitLab a plus

Qualifications

• 3+ years of experience working as a developer
• Experience with AWS and serverless architecture
• Experience with iOS, React native, PWA's
• Experience working with health care data

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Program Operations Director for the Biostatistics, Bioinformatics and Epidemiology (BBE) Program within the Vaccine and Infectious Disease Division (VIDD) at Fred Hutch oversees a comprehensive and complex array of program activities for an annual portfolio of over $30M in direct cost revenue and administrative operations including strategy, financial, grants and contracts, regulatory and administrative functions for a broad program comprised of separate but linked departments.

This position works with senior scientific leadership to translate science into strategy while responsible for the overall operations of administration, finance, grants and business analytics for the program. This position requires an understanding of federal regulatory requirements, performance management, administrative systems and program management, and broad experience with a range of business functions and systems, including program leadership, strategic planning, budgeting, fiscal analysis, human resources management, and communication. This position reports to the Senior Operations Director for VIDD.

Responsibilities

Works with overarching guidance from Principal Investigators (PIs) and the Division’s Senior Operations Director to independently plan and oversee administrative operations. Works through subordinate managers to ensure consistent, efficient and compliant administration of all work units within the program. Sets functional strategies and objectives on operational plans that align with overall Division and organizational strategies. Provides input to Division-level strategic planning. More detailed responsibilities include:

Program Oversight

1. Develop and manage all BBE Program activities to ensure compliance with all federal, sponsor and Fred Hutch requirements and guidelines and ensure operational consistency across the program
2. Provide effective and inspiring leadership by being actively involved in all programs, developing a broad and deep knowledge of all aspects of operations
3. Supervise staff, including, hiring, training, mentorship, evaluating performance, handling disciplinary action, layoff and termination issues
4. Oversee grant support activities for the program including: grant preparation, budget development/management, forecasting, reporting and report tools development
5. Ensure the adherence to regulatory compliance procedures throughout the program
6. Through subordinate managers, direct administrative activities for the program including: oversight of agency site reviews, human resources management activities, training and communication of Center policies, and administrative process improvement
7. Apprise VIDD leadership of programmatic activities, challenges and accomplishments regularly

Strategic Planning

1. Working with faculty and leadership from BBE, VIDD and the Center, create strategic plans and implement processes to achieve the initiatives and objectives set forth in each plan
2. Participate in groups and committees across the Division and/or Center to support strategic and process improvement initiatives
3. Synergize with other programs and participate in strategic planning for the Division
4. Develop and implement a system for tracking and reporting on the progress of strategic plan implementation
5. Plan and facilitate quarterly meetings for the Strategic Alliance within BBE that brings a leadership team together across multiple network grants 

Faculty Support

1. Coordinate faculty recruiting activities for the program and support the Division office in administration of faculty promotions
2. Assist the BBE Program Head in planning all BBE faculty meetings; attend program meetings and events to stay abreast on all milestones, activities and needs for the BBE faculty
3. Support faculty in cultivating and managing relationships with public and private funders to secure and expand recurring revenue streams
4. Assist the Fred Hutch Philanthropy and Marketing departments in cooperation with the Division to ensure all BBE achievements and donor relationships are appropriately highlighted and managed
5. Seek new funding opportunities for the program as appropriate

Program Operations/Other

1. Oversee financial operations for the program including: forecasting, management, reporting, reconciliations, purchasing, and vendor contract management
2. Contribute to space allocation and planning decisions
3. Oversee the HR systems and practices within BBE
4. Provide financial and overall business strategy advice to program leaders and teams
5. Participate in Division and Center-led meetings and committees and special projects
6. Other duties as assigned

Qualifications

Minimum qualifications:

• Bachelor’s degree in business, public administration or a related field
• Minimum of 8-10 years of federal research administration management experience
• Minimum of 3-5 years of supervisory and leadership experience
• Demonstrated success managing and engaging diverse stakeholders across a complex research portfolio
• Experience with translating science into strategy in creating and executing strategic plans
• Strong communication and budgetary skills

Preferred qualifications:

• Master’s degree preferred
• 3-5 years of experience in supporting faculty in an academic environment
• Experience identify areas for process improvement and implementing associated change management strategies to successfully rollout and sustain initiatives

Key skills and abilities:

• Excellent written and verbal communication skills
• Strong background in data analytics and visualization
• Advanced experience with Microsoft suite (Excel, Powerpoint, Access, SharePoint, etc)
• Ability to create a positive work culture
• Flexibility and adaptability
• Ability to multi-task in a fast-paced environment
• Outstanding interpersonal skills
• Positive attitude and sense of humor

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The director will lead the Fred Hutch Cellular Imaging Core Facility team and will be responsible for all aspect of the core functions, including providing outstanding imaging services and support to Fred Hutch investigators, scientific collaborations, strategic planning, acquisition, development and dissemination of new technologies. The resource provides equipment and expertise to assist investigators in applying sophisticated light and electron microscopy techniques.

The mission of the Cellular Imaging Shared Resource is to accelerate cancer and fundamental research for Fred Hutch/UW Consortium researchers by providing state of the art imaging and image analysis technologies, and by providing expertise on the use of such technologies and how to apply them to a variety of research projects. More specifically, the Resource evaluates current and future needs, evaluates new technologies and their potential benefits for research at the Center, obtains funding for the purchase of needed instruments, hardware and software, trains users, provides assistance with the utilization of all available technologies, provides specialized services, and disseminates and promotes the use of imaging and quantitative image analysis techniques through demonstrations, workshops, and seminars.

Responsibilities

Scope of Responsibilities

The Core Director of Cellular Imaging reports to the Associate Vice President of Shared Resources and works independently in supervising resource operations and staff. Strong interpersonal and communication skills are used in interacting with users and in promoting the resource. Expected to work under limited supervision and exercise considerable judgment and initiative in duties and responsibilities.

Major Job Duties

Research & Collaborative Development

• Identify, consult, and develop areas of collaboration for the core facility with faculty and industrial partners. Work with investigators to develop innovative applications for imaging technologies, assisting and collaborating in experimental design.
• Identify equipment grant opportunities and develop/submit grant to acquire new technology/instrumentation for the core.
• Work with researchers on individual equipment and/or image analysis grant opportunities to supplement the core.
• Develop collaborative relationships with appropriate faculty members and partner with industry to bring in new technology.
• Keep current in the field by maintaining contacts with colleagues, attending conferences and training sessions.

Leadership

• Elevate and maintain the core facility’s status as the premier scientific imaging core in the Pacific Northwest.
• Lead by example, demonstrate good judgment and transparency, get the best out of the core team.
• Responsible for developing and implementing a strategic plan for the core facility in collaboration with core facility users and advisory committee.

Service

• Engage and maintain positive working relationship with users of the core facility.
• Work with researchers to determine and guide appropriate imaging strategies for specific experiments and/or research projects.
• Communicate effectively about the services/resources available within and outside the institution to increase user base.
• Effectively address potential researcher concerns – including determining the cause of the problem; selecting and explaining the best solution to solve the problem; expediting correction or adjustment; following up to ensure resolution.
• Work with Morphometrics/Image analyst to determine instrumentation and/or imaging limitations that need to be considered for image analysis development.
• Help researchers obtain preliminary data for grants using existing imaging technologies and/or image analysis software.
• Provide support letters for investigator research grant applications.

Education & Training

• Develop and maintain a microscopy training program that utilizes existing expertise and provides users with a solid foundation for Core utilization and troubleshooting.
• Conduct demo/workshops demonstrating capabilities of existing imaging equipment and analysis software.
• Conduct demo/workshops demonstrating novel technology in partnership with industry.
• Appropriate guidance and education for individual users to meet their research needs.

Operations

• Oversee daily operation of the laboratory.  Delegate and oversee staff assignments.
• Work with Shared Resource Administration to project and develop annual resource budget. Operate and maintain the core facility budget. Manage operating budgets including the development of financial projections and business cases for each facility. Evaluate work flow and service levels, develop policies and procedures to optimize work flow and deliver high quality service. Maintain cost effectiveness.
• Work with Shared Resource Administration to establish fee schedules and policies for Center and outside users.
• Working with SVP and SR Administration, develop/establish and execute a business plan for the core.
• Generate reporting metrics on facility deliverables and service levels to advise Scientific Leads and Core Facilities Committee. Lead the process to meet annual reporting requirements.
• Interface with researchers and advisory committee to identify future instrumentation needs for the core.
• Supervise and ensure the accuracy, completeness and timeliness of record keeping including: schedules, instrument log books, records of user activity, personnel and staff time, supply inventories, purchase orders, equipment use and maintenance, metric reporting and monthly billing.
• Development and monitoring of an effective staffing and retention strategy, including hiring and terminating employees, mentor and provide learning and development opportunities for direct reports, collaborate with human resources business partners to meet the talent management goals. Provide support and guidance to team members regarding Fred Hutch policies and procedures, organizational programs, and personnel issues.

Perform other responsibilities as required.

Qualifications

Minimum Qualifications

Must have the knowledge and skills typically acquired through the completion of a PhD in Biophysics, Molecular Biology, Genetics or related field, with 3-5 years related experience. Demonstrated expertise in advanced imaging techniques e.g. confocal and two photon microscopy, light sheet, super-resolution, and/or electron microscopy. Demonstrated ability to integrate multiple types of research approaches. Strong organizational skills, attention to detail and accuracy and the ability to work in a team environment are essential.  The individual will have excellent communication skills for interfacing with expert and non-expert users, as well as lay audiences.  Proven customer service and end user support experience.

Required Qualifications – Experience, Education, Knowledge & Skills

• Ph.D. (or equivalent experience) in related science and/or engineering field
• Demonstrated research experience
• 3-5 years of experience in managing a program/team
• Peer-reviewed publications with a focus on advanced microscopy

Preferred Qualifications – Experience, Education, Knowledge & Skills

• Demonstrated experience for teaching and collaboration
• Demonstrated experience in acquiring external funding

The successful candidate will:

• Have excellent oral and written communication skills
• Be self-directed and highly motivated, capable of working independently yet in a large, interdisciplinary research environment
• Be committed to maintaining a positive work environment and fostering the establishment of new research directions/funding
• Work effectively with diverse populations
• Work independently on a wide variety of tasks and in different roles
• Work productively in a team-oriented environment and have a proven track record of team work
• Maintain effective attention to detail, meet deadlines, prioritize competing demands, and should be skilled at prioritizing, organizing, and working on multiple projects

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Hutch Data Commonwealth (HDC) is a transformative initiative at Fred Hutch that is working to bring innovative big data capabilities to the fingertips of all Hutch investigators. Specifically, HDC is developing infrastructure for the management and analysis of research data at large scale and in partnership with the Translational Data Science Integrated Research Center (TDS IRC) support investigators seeking to conduct data-driven projects and works collaboratively with center scientists to identify and source appropriate datasets, develop tools for accessing and visualizing data, and implement analytic approaches that are reproducible and responsive to scientific objectives.

Responsibilities

The Director, Data and Analytics directs the ongoing development of research data platforms and associated data and analytics services within the HDC and leads a team of data engineers and data analysts. In partnership with Product Engineering, the Data and Analytics team will enhance the analytic capability of the Center’s investigators through the introduction of innovative techniques and technologies such as machine learning, natural language processing and advanced data visualization. As part of the HDC leadership team, the Director will contribute to strategic planning, organizational development, and effort prioritization.

The Director, Data and Analytics should have strong data infrastructure and data architecture skills, a proven track record of leading and scaling data engineering teams, strong operational skills to drive efficiency and speed, strong project management leadership, and a strong vision for how data and analytics can proactively accelerate the work of Fred Hutch. Most importantly, the Director, Data and Analytics will have a passion for applying their skills in support of mission-driven research.

CORE RESPONSIBILITIES

Leadership:

• Lead a team of Data Engineers and Data Analysts and Machine Learning Engineers in the development and support of new infrastructure and data service initiatives
• Oversee recruiting, hiring, all aspects of performance management, coaching and mentoring of team members, employee development
• Build a collaborative, transparent culture of trust where team members are empowered and inspired to do their best work
• Develop team members to be able to operate in a fast paced, lean product development environment
• Be a consistent example of the center’s commitment to workplace respect, diversity and inclusion, and research integrity

Data and Analytics:

• Continually assess needs of the center’s computational community and guide the development of appropriate data resources and services
• In partnership with the TDS-IRC identify new technology and analytic tools to advance research activities
• Own the technical roadmap for HDC data infrastructure
• Manage and lead the production support aspects of data flow into HDC platforms
• Protect data integrity and accuracy; work with data source owner to increase quality and accuracy of source data
• Makes decisions, often difficult and/or unpopular, that support the goal of efficient data normalization and ETL process; influences others to support the decisions.
• Identify, evaluate and implement cutting edge big data pipelines and frameworks required to provide requested capabilities to integrate external data sources and APIs

General:

• Foster strong relationships with key teams outside of HDC, including Information Security and Information Technology
• Stay current with emerging technologies and industry trends
• Collaborate with researchers and clinicians to identify high-impact opportunities for data science applications
• Help researchers understand and utilize HDC data resources
• Ensure adoption of established best practices

SUPERVISION EXERCISED

10-12 data engineers and data analysts

Qualifications

Minimum qualifications:

• Masters or PhD degree in Bioinformatics, Statistics, Biostatistics, Mathematics, Computer Science, Physics, or equivalent required, with a minimum of five years of related experience, including a minimum of two years in a management position
• Demonstrated experience working with biomedical (clinical or research) data
• Experience with messy, “real life” data sets

Technical skills:

• Proficiency in R or Python.
• Knowledge of statistical analysis, machine learning and predictive modeling
• A variety of data formats and markup languages (e.g. XML, JSON, Markdown)
• Common data storage mediums (e.g. SQL, Excel, Access) as well as NoSQL models
• Unix/Linux and distributed computing
• Experience with source control instruments such as GitHub and related devOps processes
• Experience with workflow scheduling/orchestration resources
• Hands-on experience with big data platforms (e.g., Hadoop, Spark) and containers (e.g, Docker)

Qualities necessary for success:

• A strong desire to explore, investigate, dig, and generally uncover patterns and puzzles in data while maintaining a strong sense of thoughtful and pragmatic solutions.
• Ability to advise investigators and management in clear language about results and new directions; strong oral and written communication and critical thinking skills are necessary for this position.
• Ability to lead multidisciplinary teams including statisticians, computational biologists, and data engineers, epidemiologists, clinicians, administrators, etc.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Institutional Review Office (IRO) functions as the central office for managing the ethical review and approval of human or animal studies conducted at Fred Hutch, with specific responsibilities for supporting the Institutional Review Boards and the Institutional Animal Care and Use Committee.  The Director ensures compliance with all external regulations, best practices, and internal policies, and serves as a liaison between the committees and the research community.  The Fred Hutch IRB is the IRB of record for the Fred Hutch-University of Washington consortium greater-than-minimal-risk oncology studies.  Through close collaboration with the committee chairs and members and the IRO staff, the Director maintains an efficient and effective operating framework for the day-to-day operations of the committees and the office. 

The Director is a key member of the leadership team of the Vice President for Research Administration and Faculty Affairs and works in close collaboration with other offices and entities that support clinical and basic science research, including Clinical Research Support, Integrated Research Centers, interdisciplinary programs, Conflict of Interest, Office of Sponsored Research, Office of General Counsel, the scientific divisions, and Center executive leadership.  The Director also works closely with counterparts at the University of Washington, Seattle Children’s Hospital, and the Seattle Cancer Care Alliance.  The Director is responsible for maintaining the voluntary accreditation status of the human and animal research programs, is a primary point of contact for federal agency inquiries and correspondence, and is responsible for the management and negotiation of institutional reliance agreements, in consultation with the Office of the General Counsel.  The Director is expected to work collaboratively with faculty leaders, individual faculty and study staff, and Division Directors.

Responsibilities

• Provide leadership and oversight to the day-to-day operations of the office and its relevant committees, proactively identifying and implementing solutions to improve efficiency, effectiveness and timeliness of office processes while maintaining rigorous scientific, ethical and regulatory compliant reviews
• Provide management and supervision to IRO staff and oversee the coordination of the activities of the review committees
• As a member of the leadership team of Fred Hutch administration and the Office of Research Administration and Faculty Affairs, keep executive leadership informed with respect to all pertinent matters related to human and animal research programs at Fred Hutch
• Assist leadership on all long- and short-term objectives and other strategies necessary to achieve the organization’s mission, goals, and objectives
• Serve as liaison between Center and federal and state agencies on matters relating to human and animal protections
• Advise on policies and procedures impacting institutional compliance with federal and state regulations pertaining to human and animal research protections
• Coordinate as necessary and participate in regulatory agency site visits and audits
• Develop quantitative and qualitative metrics along with stakeholder feedback and benchmarks to measure operational performance and identify opportunities for performance improvements
• Maintain expert knowledge of all federal and state regulations pertaining to human and animal research
• Serve as a mentor to IRO staff, overseeing and supporting their professional growth, evaluating their performance and improving the quality of their work
• Oversee the implementation and maintenance of electronic systems, including the Huron IRB and IACUC products
• At all times understand and exemplify the mission and values of Fred Hutch
• Perform other related tasks as assigned or needed

Qualifications

• Bachelor’s degree with minimum of 10 years of directly relevant experience; or, an advanced degree (i.e., MPH, JD, PhD) with 7 years of experience, preferably in an NCI-designated comprehensive cancer center and/or academic medical center.
• Significant demonstrated achievement in research and staff management in a complex organization.
• Expert knowledge of research-related policies and regulations., including FDA, human and animal research protections, federal grants policy, and conflict of interest.
• Excellent interpersonal, oral, and written communication skills.
• Must be highly detail-oriented and organized with intermediate knowledge of Microsoft Word, Excel, Outlook, PowerPoint, and SharePoint.
• Demonstrated capacity to manage highly sensitive and strictly confidential material.
• Ability to solve complicated, sensitive, confidential issues quickly in a fast-paced environment.
• Self-starter, able to work under minimal supervision.
• Thorough understanding of the goals and mission of Fred Hutch.

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The mission of Internal Audit is to enhance SCCA’s operational capabilities by providing independent, risk-based and objective assurance, advisory and educational services. To achieve this, the Director of Internal Audit, reporting to the Chief Integrity Officer, is responsible for providing leadership, direction, and management of all aspects of the internal audit function through a systematic and disciplined approach to identify risks, monitor compliance with internal controls, evaluate whether such internal controls/governance practices are working effectively, and educate and train staff. This position will participate with, and support the Chief Integrity Officer in, the continuous risk assessment process and in the development and maintenance of the Internal Audit plan approved by the Board’s Integrity Committee.

Responsibilities

• Coordinate the risk assessment process ensuring it is effective, collaborative and inclusive. Analyze the risk assessment results against the organization’s strategic goals, financial impact, and the external environment to support the development of the annual risk-based audit plan.
• Develop the audit plan by prioritizing identified risks against available audit resources and create the audit plan documentation for presentation to executive leadership and to the BOD Integrity Committee.
• Continuously monitor for changes in the organizational risk profile and/or operational environment and make recommendations to modify the annual plan and to accommodate management requests for additional audit and advisory work.
• Oversee completion of the Audit Plan. Approve audit & advisory project scoping. Evaluate the risk impact of control weaknesses identified including the identification of potential systemic issues. Be accountable for timely completion of projects.
• Assure management accountability on audit risk mitigation strategies. As appropriate, assist management in implementation of risk mitigation action plans. Monitor status of open management action plans providing regular communication to the Chief Integrity Officer. Escalate concerns when risk mitigation efforts are insufficient or impacted by organizational or other changes.
• Act as primary client contact for Audit Plan related concerns & questions. Meet regularly with management to stay abreast of changes and emerging risk. As needed, support audit staff or external resources with difficult client interactions.
• Prepare reports to key stakeholders including executive management and the BOD Integrity Committee. Provide presentations to key stakeholders on audit approach, findings, and risk mitigation as requested by the Chief Integrity Officer.
• Conduct consulting activities and assistance with special project initiatives at the direction of the Chief Integrity Officer.
• Conduct training and education as opportunities are identified through assurance and advisory work.
• Support the development, implementation and maintenance of audit practices, standards, documentation and tools. Maintain awareness of changes in auditing principles and practices and related areas in order to maintain professional competence.
• Manage the process of hiring, developing, and evaluating performance of staff and manage external resources effectively.
• Other duties as assigned.

Qualifications

Required

• Bachelor’s Degree in Business Administration, Accounting or related field;
• CPA or CIA;
• Minimum 7 years audit experience with a minimum of 5 years in the healthcare industry;
• Minimum of 3 years’ experience managing audits, including risk assessment, planning, audit execution, issue/report writing, managing timelines, and management interaction.
• Excellent verbal and written communication skills
• Ability to manage significant complexity and ambiguity
• Demonstrated project management, organization and facilitation skills
• High level of personal integrity, and the ability to professionally handle confidential matters and exude the appropriate level of judgment and maturity

Preferred

• Advanced degree such as Master’s in Accounting, Business Administration, Finance, or related field.
• High level of tact and ability to communicate complex and potentially sensitive issues to various levels of management. Excellent presentation, relationship building and interaction skills. Ability to communicate effectively with all levels of leadership.
• Strategic thinker with outstanding analytical and problem-solving capabilities.
• Ability to effectively prioritize and execute tasks in a high pressure environment.
• Solid strategic thinking, business risk awareness, and appropriate judgment to use a risk-based approach in planning the audit focus.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Diversity, Equity and Inclusion (DEI) Director reports to the Executive Vice President/COO and meets regularly with other members of the Executive team, President/Director of Fred Hutchinson, and the Vice President/CHRO. The DEI Director is responsible for leading the organization’s Office of Diversity, Equity, and Inclusion, creating the overall strategy regarding Diversity and Inclusion, partnering with our Faculty Director of Diversity, Equity, and Inclusion, coaching and consulting with leaders at all levels, and sponsoring organization-wide development efforts such as Employee Resource Groups and training. Successful candidates will have the ability to work effectively with internal stakeholders and step into a leadership space as they present to staff groups, senior leaders and the Board. They must also interact effectively with external organizations and stakeholders.

The Diversity, Equity and Inclusion Director solicits direction and assistance from the Executive Vice President/COO and other key executive stakeholders involved with organization-wide strategy and leadership development, and facilitates DEI work across the entire organization. Providing guidance and coaching to various leaders conducting DEI work ensures that these local stakeholders remain engaged and accountable for their commitments.

Responsibilities

General Duties

• The Diversity, Equity and Inclusion Director collaborates with multiple leaders throughout the organization to promote the importance of diversity and inclusion to the Center’s mission and to establish and attain divisional and departmental goals in service to the organization’s overall diversity, equity and inclusion plan. The Director ensures that the diversity and inclusion work is effectively planned and implemented and will represent the Hutch’s efforts to the Board of Trustees and outside organizations.
• Manage DEI program coordinator.
• Represent Fred Hutchinson DEI initiatives at key events and national conferences (AACR, SACNAS, ABRCMS, CEO Action Pledge on Diversity & Inclusion)

Program Operations

• Serve as primary liaison to center leaders involved in diversity, equity and inclusion efforts and represent the program to outside institutions.
• Serve as a partner and collaborator with key stakeholders and center faculty in assessing and evaluating the diversity and inclusion deliverables.
• Oversee and maintain the established center-wide Diversity, Equity and Inclusion strategic plan which includes goals and accountability assignments for all areas of Fred Hutchinson.
• Curate and sponsor internal education pertaining to DEI, including topics focused on anti-racist and anti-bias behavior, upstander training and other topics determined as crucial.
• Ensure that DEI efforts are vibrant and positively impact the diverse and inclusive culture of Fred Hutch, including leading the DEI Community of Practice, managing and supporting Employee Resource Groups, the Faculty Diversity & Inclusion Committee, the Executive Diversity & Inclusion Council, Dr. Eddie Mendez Symposium and the campus-wide Diversity, Equity & Inclusion Advisory Group.
• Ensure diversity and inclusion strategic plan deliverables are accomplished, and report on KPI’s on a regular cadence.
• Bring together center diversity, equity and inclusion leaders at least twice annually to communicate/coordinate overall planning and enhance collaboration
• Act as a central repository for center, regional and national diversity demographic information in diversity and inclusion efforts, metrics and progress reporting.
• Conduct ongoing research of best practices regarding diversity, equity and inclusion work and collaborate with leaders throughout the organization to align center efforts to these practices.
• Provide updates to senior leaders and the Board of Trustees regarding diversity and inclusion efforts.
• Along with other center diversity and inclusion leaders, represent the Hutch through relevant outside organizations and engage with regional diversity/inclusion leaders.
• Curate opportunities for the workforce to develop skills to nurture and scale a diverse and inclusive workplace, including developing, sponsoring and potentially delivering workshops and overseeing the DEI Communities of Practice
• Collaborate regularly with DEI consortium partners such as the UW in joint educational programs.
• Oversee certain partnership and sponsorship requests from organizations focused on supporting diverse and underrepresented communities.

Qualifications

• A Bachelor’s degree is required (or equivalent experience in research or academic administration); an advanced degree, including JD degree is preferred 
• A minimum of 5 years of leadership and strategic program management experience, preferably in a non-profit research or academic setting 
• Ability to manage, coach, and mentor individuals and teams
• Ability to lead without direct authority
• Demonstrated knowledge of, and experience in working, on issues of diversity, equity, and inclusion through past paid or volunteer work
• Strong leadership qualities and skills are essential; collaborative teamwork, credibility, people development, sound judgement, high degree of integrity and creative problem solving
• Demonstrated ability to effectively collaborate with faculty, staff and students across all levels
• Proven ability to handle confidential information with discretion.
• Knowledge and understanding of the boundaries between DEI and Human Resource issues
• Excellent written and verbal communication skills are essential, as are demonstrated ability to manage multiple, complex and competing activities. Strong public speaking skills and presence required.

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The Safety & Emergency Preparedness Department manages a comprehensive health and safety program including: Employee Health & Safety, Fire & Life Safety, Environmental Health & Safety, and Emergency Preparedness

The Environmental Health & Safety (EH&S) Specialist develops and supports a comprehensive and integrated EH&S program at SCCA. The position is responsible for making independent decisions that lead to the development and delivery of an efficient department to meet safe environment of care standards for patients, visitors, staff and affiliates that work in or enter any SCCA facility.

Responsibilities

• Support industrial hygiene projects/design and provide safety training for labs and healthcare clinic staff, conduct exposure monitoring, respiratory fit testing, safety audits, evaluate use of hazardous materials, prepare reports and present findings to safety committee and Environment of Care committee as directed.
• Arranges, contracts, and collects/consolidates waste disposal in accordance with all applicable local, state, and federal regulations. Maintains and improves waste minimization practices to decrease hazardous materials disposal costs and comply with waste minimization regulations.
• Advise/train employees regarding the proper storage of hazardous chemicals and compressed gases, and the preparation of hazardous wastes for disposal and transportation of non-waste hazardous materials.
• Oversees the activities of consultants and vendors who provide hazardous waste services, including but not limited to biomedical waste, radioactive waste, chemical waste, electronic waste, recycled wastes, lab coat services, and spill response.
• Develop and maintain industrial hygiene, biosafety, and hazardous waste handling, transport, and disposal policies and procedures in accordance with all applicable regulations.
• Consult with employees regarding recognized and potential occupational exposures and investigate occupational accidents and illness as necessary.
• Support as needed the chemical, biosafety and radiation safety laboratory audit programs.
• Serves as Environment of Care committee member and process owner for the Hazardous Materials Management Plan and Hazard Awareness Management Manual (HAMM) and other relevant policies, as required by the Joint Commission.
• Maintains all hazardous materials program records and permits, prepares and submits required reports, and acts as site contact for applicable regulatory compliance inspections.
• Initiate and serve as a member of hazardous materials response team, maintaining written plans, procedures, and applicable training.
• Oversees the hazardous chemical inventory process and database, verifying that data is accurately maintained and that quantity limits in designated areas do not exceed fire code storage limits.
• Provides training employees on various topics including hazardous waste disposal, shipping hazardous materials, spill response, and waste minimization.
• Will require limited off-hours support
• Perform other duties as required.

Qualifications

Required:

• BA/BS in related field (5 years similar experience may substitute)
• 2+ years similar experience, preferably in healthcare/labs

Preferred:

• Bachelor’s degree in industrial hygiene, environmental health, chemistry, microbiology or closely related scientific field
• Experience supporting biosafety programs a plus
• Must possess good writing, analytical, verbal communication and computer skills
• Must be able to work independently
• Must be able to wear a respirator and required personal protective equipment
• Must be capable of lifting 40 pounds

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

Responsibilities

A clinical Epidemiology group in the Vaccine and Infectious Disease Research Division is recruiting a doctoral-level epidemiologist to work on the Cervical Cancer Prevention Partnership (C2P2) project. C2P2 is a collaboration between investigators in the United States, Peru, and Brazil, with the following two goals:

1. building strong collaborative partnerships, and
2. conducting clinical trials in Peru and Brazil to address the cervical cancer prevention and treatment needs of HIV-infected populations.

A primary component of the C2P2 project is an upcoming randomized clinical trial of HIV vaccination among HIV-positive adolescents in Peru and Brazil. The candidate will be expected to develop study protocols, standard operating procedure (SOP) documents, produce data collection instruments such as case report forms (CRFs), and produce documents and consent forms for submission to IRB for approval. The candidate must be responsible, organized, and self-motivated, and able to efficiently manage time and experiments.

Qualifications

A PhD in epidemiology, biostatistics or a related field is required for an hourly position (~30-50% time). The candidate must show initiative, the willingness to take up new skills and responsibilities, and be a team player. Excellent attention to detail and the ability to work independently are essential to success in this position, as are good communication and organizational skills. Experience working on clinical research studies, particularly the following: protocol development, developing and writing SOPs and data collection instruments, generating and updating IRB applications and working with IRBs, required. Demonstrated understanding of epidemiologic methods and clinical trial design and methods required. Spanish language skills and experience with research conducted in Latin America preferred but not required. Salary will be commensurate with (appropriate) experience. 

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Executive Assistant supports the Vice President & Chief Human Resources Officer and represents the Human Resources office in interactions both internally and externally. An essential member of the Human Resources staff, the Executive Assistant will anticipate needs, clear obstacles and identify opportunities to take ownership of tasks and projects. The Executive Assistant is expected to take initiative, proactively ask questions, execute core responsibilities collaboratively, and work well within a complex organization. Must maintain professionalism, show flexibility, handle multiple tasks and changing priorities, be customer service oriented, have a strong attention to detail, and remain composed under pressure of deadlines. The Executive Assistant must be able to effectively communicate the mission, values, and scope of the institution.

Responsibilities

• Manage a constantly changing executive calendar for Vice President & Chief Human Resources Officer and triage incoming requests and correspondence.
• Provide meeting support by looking ahead and anticipating needs for creation of agendas, PowerPoint presentations, handouts, and dashboards.
• Manage relationships with executives, high-level donors, board members and key contacts, ensuring timely follow-up and scheduling.
• Create and edit internal communications, including written communications to executives, directors, managers, and all staff.
• Provide thorough and detail-oriented planning and support to executive-level meetings and special events including logistics, materials, presentations, taking minutes, and follow-up on action items.
• Assist in the onboarding of new HR staff and maintain HR organizational chart accordingly.
• Support People Operations and Culture Manager in assisting with multiple Fred Hutch executive leadership development initiatives and HR teambuilding events.
• Manage travel arrangements, itineraries, and monthly credit card reconciliations.
• Other duties as assigned.

Qualifications

Minimum Qualifications

• Bachelor’s degree or equivalent administrative experience.
• 5-8 years progressively complex administrative work supporting a Vice President or C-level executive.
• Advanced proficiency in Microsoft Office Suite in both PC and Mac platforms.
• Must be organized, detail-oriented, and have experience in event and project coordination.
• Able to efficiently prioritize multiple tasks, use independent judgement to troubleshoot, and thrive working with and helping people.
• Demonstrated ability to work in a team environment and meet goals in a timely manner.
• Highly developed organization and information management skills.
• Strong writing and editing skills.
• Ability to communicate clearly and concisely, both orally and in writing.
• Strong attention to high level of detail and quality of work.
• Commitment to delivering excellent customer service.

Preferred Qualifications

• Prior work experience in Human Resources.
• Willing to ask for direction or ask questions if given unclear projects or tasks.
• Experience handling confidential and sensitive information.
• Solid background in planning travel, meeting agendas.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The role of the Staff Facilities Engineer is to protect Fred Hutch's investment in complex research facilities by maintaining facilities engineering design integrity and making improvements where possible. The Staff Engineer provides technical engineering support to facilities operations, facilities alterations, and new capital development projects at all Fred Hutch locations.

The Engineer reports to the Director of Facilities Engineering and works with the Facilities Engineering Department to serve Engineering operations and maintenance staff, Facilities Planning, Environmental Health and Safety, Construction Administration, and others in providing an effective research environment in support of the Center’s mission. The Engineer evaluates physical plant aspects of facilities alterations and new facilities construction. The Department operates and maintains 1.6 million SF of technologically advanced research facilities including 5 different power plants, 13 data centers, Biologics and Cell Production Facilities and a state of the art clinic that serves 500 patients each day. This position is instrumental in defining new building standards for reliable operations and energy efficiency.

Responsibilities

The Engineer supports the Facilities Engineering in operating and maintaining Fred Hutch facilities. Physical plant systems include steam and hot water boilers, specialized laboratory utility systems, air handling systems, chillers and chilled water system, HVAC, power transformation and distribution, emergency generator, and building automation controls. The Engineer will:

• Develop procedures to operate and maintain critical utilities distribution systems.
• Analyze systems operation and make recommendations for improvement. Work with Operating Engineers to establish and document effective operating procedures.
• Assist and advise Operating Engineers in trouble shooting systems operational problems. Conduct special investigations, tests, and other studies to improve efficiency and reliability of equipment and systems.
• Review and analyze equipment maintenance procedures and help establish Operating Engineer training.
• Support preventive maintenance and predictive maintenance programs. Review procedures. Analyze equipment histories and downtime records. Inspect equipment and develop renewal and replacement program.
• Investigate Indoor Air Quality complaints when HVAC design or air balancing are in question.
• Implement an energy measuring and reporting system and make recommendations for energy usage reduction.
• Coordinate with public utilities for optimum reliability and cost of service.
• Maintain drawing and document control and facilities standard specifications.
• Manage physical plant improvement projects.
• Develop engineering specifications for equipment repair, replacement, or modifications.
• Prepare spare parts and critical spares justification analysis.
• Keep current on code requirements and modern engineering techniques to support operations and maintenance programs.
• Review capital equipment purchase requisitions for compatibility with building systems.
• Assist in facilities disaster planning.
• Assist with field commissioning tests and inspections. Write or assist in writing commissioning procedures.
• Lead and assist Operating Engineers and/or outside consultants in air balancing of laboratories and other facilities.
• Support major service contracts. Develop specifications and inspect work.
• Support periodic major maintenance and overhaul of equipment including boilers and chillers.
• Support Engineering budget planning and control.
• Carry “on call supervisor” Pager in rotation with other Facilities Engineering staff.

Alterations Support:

Facilities alterations usually involve complex HVAC and building automation controls modifications.

• Assist Facilities Planning in project development and budgeting.
• Review physical plant aspects of alteration projects. Develop specifications and work with consulting engineers and contractors as required by project scope.
• Prepare engineering bid packages as necessary.
• Inspect installation.
• Lead start-up and commissioning efforts.

Capital Development Support:

The Engineer will represent the Engineering department in reviewing new facilities engineering design.

• Assist with new construction inspection and component testing.
• Actively participate in start-up and commissioning activities.
• Provide training of Operations Engineers in the operation of the new facilities.
• Develop operations manuals for use by the Department.
• Provide feedback to the design team on operational problems in existing facilities.
• Manage capital projects in progress.

Qualifications

• Bachelor of Science in Mechanical Engineering is required unless advanced skills and experience can be demonstrated as equivalent to education requirement
• Four or more years of increasing responsibilities at the professional level in HVAC, Controls and Plumbing engineering design with knowledge of maintenance and operations for large bio-medical research or hospital facilities is required
• Emphasis will be in the areas of laboratory design, construction and operation
• Design and field experience in HVAC, boilers, and DDC automated building control systems and experience in electrical distribution systems operation and maintenance is required
• Project management experience in mechanical, electrical, and piping projects is preferred
• Current Washington State Professional Engineering license is desirable

The Fred Hutchinson Cancer Research Center invites applications to fill a full-time laboratory-based faculty position. Located in the vibrant South Lake Union neighborhood of Seattle, Washington—Fred Hutch is home to three Nobel laureates, over 300 faculty, and 2400 staff. Our interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose, and treat cancer, HIV/AIDS, and other life-threatening diseases.

We are recruiting a virology, microbiology, or immunology faculty member wishing to establish an independent lab working on a virus or bacteria that is associated with cancer. Applicants from PhD, MD/PhD, or MD scientists will be considered at any rank. Successful candidates will align with the objectives described below.

The Pathogen Associated Malignancies Integrated Research Center faculty are dedicated to accelerating innovation through interdisciplinary science through these objectives:

(1) understand basic mechanisms of host-pathogen interactions of pathogen-associated malignancies (PAMs) to identify mechanisms of cancer induction and exploit vulnerabilities

(2) support translational studies of PAMs to inform the design of better diagnostic, and/or therapeutic strategies

(3) research and implement prevention strategies for PAMs.

Our researchers focus on Human Papilloma Virus, Merkel Cell Carcinoma, Kaposi's sarcoma-associated herpesvirus (KSHV), Epstein-Barr Virus and EBV-related cancers, liver cancer, as well as the role that specific microbes play in the etiology of cancers and response to treatment. We are seeking to expand research on PAMs, including Hepatitis viruses. 

The successful candidate will enter a dynamic, collaborative research environment, working across Fred Hutch’s many diverse Divisions including Human Biology, Basic Sciences, Clinical Research, Public Health Sciences, and Vaccine and Infectious Diseases. Opportunities exist for University of Washington affiliate appointments, participation in joint UW-Fred Hutch graduate student programs, collaboration with the Immunotherapy Integrated Research Center and with clinicians practicing at the Seattle Cancer Care Alliance—one of the leading cancer treatment centers in the United States.

Please submit your application by providing a curriculum vitae, a 2 to 3-page research plan, three recent publications, and three letters of reference.

The applicant review process begins as applications arrive and any application received by October 30th, 2019 will be guaranteed consideration for the position.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Financial Analyst II position supports the fiscal management operations of the Infectious Disease Sciences (IDS) Program. The position collaborates with internal and external stakeholders and partners including Principal Investigators, program, division and center staff, and sponsor organizations to ensure timely and accurate accounting and financial reporting of sponsored research in compliance with federal and external sponsor regulations and requirements. This position will co-manage the preparation, interpretation and analysis of financial data, and is responsible for the management and administration of sponsored and non-sponsored research project funds.

Responsibilities

The incumbent works with minimal supervision and reports to the Fiscal Manager in the Infectious Disease Sciences Program. The Financial Analyst II (FA) will design, develop, and be responsible for overseeing and managing budget/fiscal systems, policies, and procedures for grant and contract budgets for Principal Investigators and management staff. They are expected to use initiative and sound judgment in carrying out responsibilities within the framework of the appropriate funding source/agencies policies and procedures. They provide highly responsive, efficient support services and has a broad range of responsibilities including: establishes and maintains comprehensive fiscal record keeping systems including: budget monitoring and reporting for grants management, subcontract oversight and special project support in support of the program. This position serves as the liaison for funding issues related to grant, contract, subcontracts, clinical trial budget management and support with an increasing workload for these types of studies in IDS. In this area of responsibility, the FA interprets and ensures compliance with sponsor (federal and industry) guidelines, and maintains and manages study payments and milestones.

1. Develop and guide cost analysis process by establishing and enforcing policies and procedures; providing trends and forecasts; explaining processes and techniques; recommending actions to PIs and program leadership. Performs professional financial and budget analysis for PIs and program leadership promoting strategic decision-making and fiscal responsibility, using research business metrics to clarify all decision making support optimal decision-making and cost management.
2. Develop, modify, and maintain multiple record keeping and reporting systems for varied and complex sources of funding. Oversee and co-manage monthly budgets to actual reporting, year-end summary analysis and trend reporting to program leadership and PIs, and analysis of significant variances at a program and project level. Utilize online financial system to monitor budgets and resolve problems. Ensure accuracy and integrity of financial information in the development of complex technical fiscal analysis and financial reporting to multiple sources according to strict guidelines and deadlines. Review project costing classification and integrity of data used in financial reports, proposing resolutions of discrepancies in financial data to management, as needed.
3. Assist in the annual budget process including analysis of submitted budgets compared to budget targets, preparation of summarization reports and communication of results to program leadership/PIs.

The position focuses on setting up of systems for industry-sponsored studies and working with Principle Investigators (PIs) and clinical research staff to maintain, monitor, track and manage study milestones and payments. Each clinical trial is unique as PIs work with a multitude of industry sponsors and each contract and study is unique based on enrollment criteria/eligibility, milestone tracking (e.g. patient visits, screen failures), complexity of reporting data, and close-out procedures.

1. Manage/monitor sponsored and non-sponsored research projects funded with restricted contributions and communicate with program leadership/PIs for project approval and set-up, budget monitoring and project close-out. This includes: working closely with teams and sub-awarding institutions on managing sub award setup, billing and payments. Conduct all necessary steps in closing out of expired budgets including cost transfers, salary transfers, and verifying that all sponsor payments have been received.
2. Oversee accounting for federal sponsored research grants, industry contracts, and other designated funds so that grants and contracts and non-sponsored research projects are managed in accordance with grantor and contractor requirements. Communicate with program leadership/PIs for project approval and set-up, budget monitoring and project close-out. This includes monitoring grant, contract, clinical trial, clinical research, foundation, operational, gift and discretionary budgets to document expenditures and verify proper accountability.
3. Monitor non-sponsored research projects funded with restricted contributions and communicate with strategic planning initiative research administrators for project set-up, budgeting and close-out.
4. Perform other financial analysis and special projects as assigned.

Qualifications

• Bachelor’s degree in accounting or finance preferred.
• Minimum of 2-5 years of experience in accounting or finance preferred, ideally in a research or not-for-profit environment.
• Exceptional analytic skills and demonstrated ability to build financial models for business forecasting, variance analysis, and problem solving and providing recommendation based on results to PI and program management for strategic decision-making.
• Advanced proficiency in Excel (including Pivot Tables), PowerPoint, Access, SharePoint and Word.
• Experience with Tableau, or similar data visualization tool.
• Well-developed verbal and written communication skills, including an ability to understand complex problems, to collaborate and explore alternative solutions. Ability to organize thoughts and ideas into understandable terminology.
• Ability to work independently on multiple projects and communicate status of projects to key decision makers on a proactive basis. Position may require flexible work hours to meet deadlines/deliverables.
• Exposure to performing grant submissions and accounting or project cost accounting a plus. Familiarity with NIH rules/guidelines.

At the Fred Hutchinson Cancer Research Center (Fred Hutch), we believe that the innovation, collaboration, and rigor that result from diversity and inclusion are critical to our mission of eliminating cancer and related diseases. We are committed to increasing our awareness and improving our practices so that we are an organization known as a center of diversity and inclusion excellence.  As a part of this effort, we are committed to advancing diversity, equity, and inclusion in scientific research and supporting the career development of the next generation of scientists. 

Overview:

Fred Hutch is seeking applications for the 2nd Annual Dr. Eddie Mendez Scholar Award which recognizes outstanding postdoctoral fellows from any discipline who are conducting research related to cancer, HIV, or other infectious diseases. The award was created to recognize Dr. Méndez’s commitment to cancer research and to supporting early-career underrepresented minority scientists and scientists with disabilities.

Awardees will arrive on May 22, 2019 and will participate in activities on campus while exploring Seattle. They will then present at a scientific symposium on May 23,2019  honoring Dr. Eddie Mendez and will have the opportunity to visit Fred Hutch and meet with faculty members.

This award recognizes the achievements of post-doctoral fellows from backgrounds that are underrepresented in science based on the NIH definition, which includes individuals from underrepresented racial and ethnic groups (Blacks or African Americans, Hispanics or Latinos, American Indians or Alaska Natives, Native Hawaiians and other Pacific Islanders), individuals with disabilities, and individuals from disadvantaged backgrounds. A selection committee consisting of Fred Hutch faculty will select up to six awardees. All expenses related to travel and accommodations will be provided by Fred Hutch.

Dr. Mendez, who died of cancer in 2018, specialized in treating head-and-neck cancer, an often disfiguring and debilitating disease. It was his mission to save lives and improve the well-being of cancer patients, whether through spearheading minimally invasive robotic surgery for these tumors (he was the first in Washington state to perform such surgery), or through tirelessly developing new treatments in his laboratory at Fred Hutch. 

Dates and Location:

Arrival: Thursday, May 22, 2019

Symposium: Friday, May 23, 2019

Where: Fred Hutchinson Cancer Research Center, Seattle, WA 

Additional information to follow. 

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The GMP Systems group is a compliance function within the Cellular Processing Facility (CPF). The CPF is a manufacturing organization that executes process operations in the production of modified cellular products for patients participating in cell therapy clinical trials in the Fred Hutch Cancer Research Center. GMP Systems is responsible for developing and administrating a variety of quality systems to ensure compliance with applicable regulations. The groups focus is on all aspects of GMP equipment life cycle, as well as on raw materials inventory management.

The GMP Systems Specialist II will primarily address facilitation of process equipment commissioning and qualification, routine calibration, maintenance, and repairs of GMP manufacturing and laboratory equipment to ensure a continued state of regulatory compliance and continuity in support of clinical manufacturing operations.

Responsibilities

• Track, schedule and ensure on-time completion of routine equipment service events.
• Establish and manage service providers and vendor contracts related to equipment maintenance, calibration, and repair.
• Maintain pertinent documentation and equipment files, including drawings, O&M manuals, equipment logbooks and service records in accordance with GMP record keeping practices.
• Facilitate shipment of equipment serviced off-site.
• Identify and communicate deviations from established procedures.
• Respond to notifications of malfunctioning equipment, participating in investigation to diagnose cause, coordinate repairs by Fred Hutch Engineering or other service provider, as necessary.
• Facilitate verification of restored performance following equipment repairs, to ensure equipment is suitable to return to service.
• Support development of equipment specifications (user requirements) for new equipment, participate in equipment selection, procurement, installation, etc.
• Facilitate commissioning and qualification of new equipment.
• Author equipment validation protocols and reports. Assist in execution of validation protocols. Investigate and document validation deviations.
• Support development of operation and maintenance Standard Operating Procedures (SOP) for new equipment.
• Assist manufacturing staff with troubleshooting and/or continuous improvement of equipment operations.
• Provide additional support for GMP equipment life cycle, as needed.

Qualifications

Minimum Requirements:

• BS in a Biological Science or Engineering, or relevant experience in biologics manufacturing and/or cellular therapeutics processing.
• Experience working in a regulated (GxP) environment, including a thorough understanding of GMP record keeping and documentation practices.
• Experience creating and revising SOPs.
• Strong troubleshooting and problem solving skills.
• Must be able to work efficiently, with strong attention to detail in a regulated environment.
• Must be able to communicate effectively in a diverse team environment in support of team goals. 
• Must demonstrate solid time management and organizational skills, with good verbal and written communication. 
• Must be able to wear appropriate clean room attire and have the ability to wear surgical masks and all required Personal Protective Equipment (PPE). 
• Meets physical requirements of the job, as follows:  must have the ability to lift a minimum of 50 pounds, the ability to bend, reach, stretch, climb ladders and work in tight spaces in order to complete job tasks.
• Experience with basic Microsoft Office Software (Word, Excel, Visio, etc.)

Preferred Skills:

• Experience working as a customer service provider.
• Experience working in cellular therapeutics and/or biologics manufacturing environment.
• Experience creating equipment SOPs for GMP clinical process equipment, and other GMP documents (reports, user requirements, etc.)
• Experience in developing and authoring equipment validation protocols and reports
• Experience in assisting with facilitation of facility start-up and shut down activities
• Strong administrative and logistics skills required to track a large variety and volume of tasks simultaneously.

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The Sales Associate is responsible for providing sales assistance to customers, assisting with merchandising, stocking, and receiving inventory and performing oncology related sales and consultations. This employee will receive and enter inventory into our Point of Sale system, contribute to marketing efforts, open and close store, process sales transactions, direct the work of volunteers and assist customers with sales. This position is located at the SCCA’s oncology retail store, Shine.

Work Schedule: Position is required to work one Saturday per month 11am-3pm. Monday and Friday 10:30am-6pm and Thursdays (if not working Saturday) 10:30am-6pm. 20 hours per week.

Responsibilities

• Receives inventory into our POS system – tagging, stocking, inventory management and transferring product.
• Processes sales transactions – assists customers, accepts payment, refunds, and exchanges. Includes opening and closing of store and till reconciliation and deposits into safe.  
• Create merchandising and product displays, both in-store and at off-site events assisting with marketing goods and services (including contributing to social media marketing efforts).
• Direct the work of volunteer staff during shifts – assigning projects and ensuring tasks are complete.
• Assist with fittings as permissible via training and competence – wigs, canes, compression products and assist with customer/patient files as requested.
• Contribute to department performance improvement efforts.

Qualifications

Required:

• High School graduate or GED
• Minimum of three years of retail sales experience
• Proficiency using a cash register/point of sale system
• Ability to enter data accurately
• Ability to provide exceptional customer service both in person and via telephone communications

Preferred:

• BA/BS in related field of study
• Quickbooks Point of Sale experience
• Experience in fitting compression garments and wigs

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Etzioni Lab in the Biostatistics Program at Fred Hutch is seeking a graduate research assistant (GRA). Under Dr. Etzioni's supervision, the GRA will work with PI or Sr. Statistical Analyst to analyze the cost-effectiveness of reflex test biomarkers to inform biopsy decisions in men found to have intermediate PSA levels on routine screening. This work will involve sourcing relevant cost and utility data, developing code for analysis, and preparing a manuscript.

Responsibilities

• Research and collect data
• Interpret, synthesize, and analyze data – potentially using advanced data modeling techniques
• Plan and modify research techniques
• Prepare reports summarizing methods and results
• Write and edit materials for publication or presentation
• Attend project meetings
• Other duties and responsibilities assigned by PI or Sr. Statistical Analyst

Qualifications

• Bachelor's degree
• Current enrollment in UW graduate program with experience and authority in the subject matter of the research project
• Oral and written communication skills to discuss and document research progress
• Ability to work independently, accurately and to problem solve technical and methodological issues that arise in the course of the research
• Knowledge and experience with statistical analyses
• R programming skills

PLEASE NOTE: This a part-time role targeted at 10 hours/week

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Hutch Data Commonwealth (HDC) at the Fred Hutchinson Cancer Center (the Hutch) drives the development of data-intensive research capabilities and infrastructure across Fred Hutch through software and data engineering, training, and strategic partnering.

We are seeking a charismatic individual with a background in bioinformatics or computational biology research to facilitate data-intensive partnerships and identify collaboration opportunities within the Hutch and with broader scientific community. A strong candidate will have knowledge of high-throughput experimental methodologies, large genomic datasets, and computational analysis to successfully describe key concepts across both technical and non-technical collaborators.The Scientific Liaison will enable high-quality science through their ability to match research needs with skill sets and personalities of potential collaborators, which may include but are not limited to: Hutch faculty, external researchers, undergraduate student interns, graduate student and postdoctoral researchers, capstone project students, and industry fellows.

The ideal candidate will be comfortable communicating across a wide range of backgrounds and levels of expertise, and will maintain strong relationships with the Hutch researcher community to better support their needs. They will be in continuous contact with researchers to fully understand their challenges and help identify partnership opportunities. This position requires excellent oral and written communication skills and a deep understanding of the research process and culture.

This role will report to the Director of Alliances and Data Strategy. The Scientific Liaison will provide input into the types and nature of institutional partnerships that would be most useful, and identify opportunities for wider impact through more intensive engagement.

Responsibilities

• Understand key aims, concepts, and methods of Fred Hutch’s research portfolio. 
• Be able to converse with researchers about their work, methods, and approaches.
• Have familiarity with commonly used approaches and methods related to data-intensive research in the biomedical space.
• Develop in-depth familiarity with researchers. Make connections between researcher needs and research outcomes and opportunities.
• Facilitate translation of collaborator requests into practical steps, and determine whether and how they are achievable.
• Make recommendations regarding the allocation of people, time, financial, and intellectual resources; track resource use and needs across projects.
• Manage, maintain, and grow an engaged network of internal and external research collaborators.
• Help with creation of job descriptions and recruiting materials related to research partnerships. 
• Monitor collaborator satisfaction and assess their needs. 
• Contribute to the strategic planning and management activities of the Alliances and Data Strategy team.
• Facilitate sharing of knowledge and best practices in data science among researchers and others at the Hutch.
• Other duties as required.

Qualifications

• PhD in biomedical sciences, computational biology, bioinformatics, or other discipline related to data-intensive research; or equivalent experience 
• Competency in data science skills, approaches, and languages like R and/or Python, SQL, machine learning, and version control
• An empathetic mindset with a deep understanding of research processes, challenges, opportunities to facilitate relationship building and trust.
• Strong oral communication skills to convey and explain information effectively and across varying audiences
• Strong organization and project management skills. Self-motivated and driven to make a difference.
• Strong interest in open science and data sharing.
• Experience in or willingness to learn product development concepts, practices, and processes.
• Intellectually curious and adept at rapidly comprehending the general goals of cutting-edge biological research and the nuances of how data science intersects with these objectives.
• Committed to working with diverse teams.
• Desirable: Experience working in communication and/or outreach to researchers. 
• Desirable: Familiarity with data formats and markup languages (e.g. XML, JSON, Markdown); common data storage mediums (e.g. SQL, Excel, Access); distributed computing; big data platforms (e.g., Hadoop, Spark); and containers (e.g, Docker)

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

Responsibilities

• Supports HIM processes, as assigned, in the areas of scanning, upload, and indexing of paper into the EHR; processing new and returning patient records; fulfilling record requests; supporting clinical teams; and other duties
• Performs other reasonably-related HIM duties, as assigned by HIM Leadership
• Assists with cross-coverage in the HIM department by training others and learning new tasks
• Responds to requests for charts and patient information from providers, clinics, and facilities in accordance with HIM policies, and Federal and Washington State law
• Reviews and validates Release of Information (ROI) forms for the use and disclosure of protected health information (PHI) according to state and HIPAA law in the performance of release of information requests
• Possesses innate ability to interact with all types of internal and external customers in a flexible and accommodating manner
• Possesses knowledge of health information management (HIM) operations and HIPAA law
• Demonstrates proficiency with computer data entry skills (EPIC, Cerner, WORD)

Qualifications

Minimum qualifications:

• Minimum 2-years of pertinent education required
• Knowledge and demonstrated proficiency of health information systems, computer software and database fundamentals required
• At least 1 year experience in healthcare environment required
• Knowledge of medical terminology required
• Demonstrated ability to exercise independent judgment in tandem with departmental policies and procedures required.
• Demonstrated ability to perform all duties with a sense of urgency required.
• Demonstrated work style to show a high level of organization and detail-mindedness required.
• Demonstrated written and verbal communication excellence with patients, clinical teams, and colleagues required.
• Demonstrated ability to handle large work volumes while sustaining accuracy required.
• Demonstrated caring and compassionate actions while supporting patient-centered care required.
• Demonstrated beliefs resulting in actions showing that "even while supporting clinical teams, our patients are our true customers" required.
• Demonstrated "self-starter" abilities in the management and oversight of day-to-day HIM operations required.
• Demonstrated ability to meet and exceed productivity benchmarks without direct supervision required.
• Demonstrated capability of multitasking between different duties with ability to quickly reprioritize tasks required.
• Other physical demands may include, but are not limited to: Sitting, standing, walking, bending, stooping, reaching, pushing, pulling, lifting, and carrying.

Preferred qualifications

• RHIT/RHIA preferred

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Seattle HIV Vaccine Trials Unit is seeking a committed, energetic person to join our community outreach team. 

Responsibilities

The Recruiter’s primary responsibilities will be to recruit participants for our groundbreaking HIV vaccine studies.  Recruitment will occur in local venues that may include street locations, community events, community based organizations, public clinics as well as bars, dance clubs, and sex clubs.  Recruitment efforts will target diverse populations according to the demands of the current studies.  Work will include some administrative duties.

Qualifications

Minimum Qualifications

• Must be at least 21 years old
• Possession of a high school diploma or equivalent
• Excellent verbal and written communication skills
• Candidates for the position must be willing to learn a variety of skills related to recruiting, counseling and providing HIV/STD health education, and details about our research studies

Preferred Qualifications

• Familiarity with gay community venues preferred
• Previous experience recruiting for clinical trials
• Previous experience working with men who have sex with men (MSM)
   

Flexible schedule will include weekday, nights and weekends on a “as needed” basis.  Knowledge of and sensitivity to youth, racial, ethnic, cultural, and sexual diversity is essential.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

Center Information Technology (CIT) is looking for an outstanding, customer-focused Cloud Product Manager to join the team.

The Cloud Product Manager II, is accountable for shepherding, launching, upgrading and life cycle management of a portfolio of cloud applications and services (medium to large complexity / scale) for the Fred hutch Cancer Research Center. Through collaboration with scientific and administrative process owners, they hold responsibility for both day-to-day operations and success of the overall product roadmap and how it aligns to the Fred Hutch IT roadmap.

Responsibilities

• Investigates, launches and maintains a portfolio of cloud products / applications (medium to high complexity / scale)
• Facilitate defining product strategy and manage the day-to-day implementation of cloud applications with different technical architectures, different hosting methods (IaaS, SaaS, PaaS)
• Creates and maintains roadmap for the products within the role’s portfolio; collaborates with key stakeholders to identify enhancements and owns the product backlog
• Distill business requirements (from high-level objective to actionable requirements) to define scope and functionality of product offering
• Drive execution of product enhancement and developmetn through the complete define / build / test / launch / review / sunset life-cycle ensuring services meet the desired business objectives
• Conduct third-party product evaluation and lead integration when necessary
• Manage operational support processes for product support, including monitoring tickets, vendor SLAs, SOWs, contract, budget and renewals management
• Own and manage product vendor relationships and licensing agreements
• Monitor performance of solutions through metrics to provide transparency into application health
• Adopts a proactive approach to identify risks to product success
• Ability to prioritize workload effectively, and thrive in a dynamic and complex environment under moderate supervision

Qualifications

• Minimum 5 years’ experience in enterprise software in either systems engineering or other customer-facing/technical related role
• Intermediate business analyst and/or project management skill set, including customer support experience
• Intermediate knowledge and experience working with different technical architectures, different hosting methods (IaaS, SaaS, PaaS)
• Intermediate ability to manage vendors, support contracts, negotiate SLAs
• Prior experience effectively leading and managing collaborative, cross-functional relationships
• Some change leadership skills (i.e., ability to effectively manage communication, negotiate successful outcomes, identify risks, engage correct stakeholders, etc.)
• Ability to build relationships with customers and discern what’s critical to them
• Ability to generate ideas for how software tools can make our customers more successful
• Excellent written, communication and presentation skills
• BS in Computer Science, Engineering or related field desired
• ITIL/ITSM foundation certified a plus

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

This position is responsible for routinely compounding and distributing medication and pharmaceutical supplies in both IV admixture and pharmacy distribution areas, in accordance with facility standards and procedures and regulatory requirements. Work is performed under the direct supervision of a pharmacist.

Responsibilities

• Accurately perform pharmaceutical calculations and prepare intravenous admixtures and any other tasks as required that relate to the dispensing of infusion therapy or as assigned
• Interact with professional staff and public on a daily basis
• Perform certain routine and repetitive functions and engage in sterile and non-sterile preparation and packaging of medications and other pharmacy related functions, under direct supervision of a Registered Pharmacist
• Maintain inventory control of pharmaceuticals
• May need to perform order entry of prescriptions into the outpatient pharmacy computer and assist in filling of new prescriptions or refills including cashiering
• Assist in training and orientation of pharmacy technicians, interns and pharmacists and be responsible for other duties as assigned

Qualifications

• Must have a current Washington State Pharmacy Technician License
• High school graduate or equivalent
• Able to work under direct supervision of a pharmacist in providing service to patients
• Able to communicate with other health care professionals, and the public in a polite and appropriate manner
• Must have proper aseptic technique experience in accurate, efficient and timely preparation of parenteral products
• Good oral and written communication skills
• Experience with computer systems and data entry
• Able to work independently in a creative and assertive manner
• Able to maintain patient confidentiality
• Able to perform basic pharmaceutical calculations
• Able to perform Pharmacy Technician functions including preparation, packaging and labeling of medication in an accurate and efficient manner

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

This position is responsible for routinely compounding and distributing medication and pharmaceutical supplies in both IV admixture and pharmacy distribution areas, in accordance with facility standards and procedures and regulatory requirements. Work is performed under the direct supervision of a pharmacist.

Responsibilities

• Accurately perform pharmaceutical calculations and prepare intravenous admixtures and any other tasks as required that relate to the dispensing of infusion therapy or as assigned
• Interact with professional staff and public on a daily basis
• Perform certain routine and repetitive functions and engage in sterile and non-sterile preparation and packaging of medications and other pharmacy related functions, under direct supervision of a Registered Pharmacist
• Maintain inventory control of pharmaceuticals
• May need to perform order entry of prescriptions into the outpatient pharmacy computer and assist in filling of new prescriptions or refills including cashiering
• Assist in training and orientation of pharmacy technicians, interns and pharmacists and be responsible for other duties as assigned

Qualifications

• Must have a current Washington State Pharmacy Technician License
• High school graduate or equivalent
• Able to work under direct supervision of a pharmacist in providing service to patients
• Able to communicate with other health care professionals, and the public in a polite and appropriate manner
• Must have proper aseptic technique experience in accurate, efficient and timely preparation of parenteral products
• Good oral and written communication skills
• Experience with computer systems and data entry
• Able to work independently in a creative and assertive manner
• Able to maintain patient confidentiality
• Able to perform basic pharmaceutical calculations
• Able to perform Pharmacy Technician functions including preparation, packaging and labeling of medication in an accurate and efficient manner

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

This position is responsible for routinely compounding and distributing medication and pharmaceutical supplies in both IV admixture and pharmacy distribution areas, in accordance with facility standards and procedures and regulatory requirements. Work is performed under the direct supervision of a pharmacist.

Responsibilities

• Accurately perform pharmaceutical calculations and prepare intravenous admixtures and any other tasks as required that relate to the dispensing of infusion therapy or as assigned
• Interact with professional staff and public on a daily basis
• Perform certain routine and repetitive functions and engage in sterile and non-sterile preparation and packaging of medications and other pharmacy related functions, under direct supervision of a Registered Pharmacist
• Maintain inventory control of pharmaceuticals
• May need to perform order entry of prescriptions into the outpatient pharmacy computer and assist in filling of new prescriptions or refills including cashiering
• Assist in training and orientation of pharmacy technicians, interns and pharmacists and be responsible for other duties as assigned

Qualifications

• Must have a current Washington State Pharmacy Technician License
• High school graduate or equivalent
• Able to work under direct supervision of a pharmacist in providing service to patients
• Able to communicate with other health care professionals, and the public in a polite and appropriate manner
• Must have proper aseptic technique experience in accurate, efficient and timely preparation of parenteral products
• Good oral and written communication skills
• Experience with computer systems and data entry
• Able to work independently in a creative and assertive manner
• Able to maintain patient confidentiality
• Able to perform basic pharmaceutical calculations
• Able to perform Pharmacy Technician functions including preparation, packaging and labeling of medication in an accurate and efficient manner

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

This position is responsible for routinely compounding and distributing medication and pharmaceutical supplies in both IV admixture and pharmacy distribution areas, in accordance with facility standards and procedures and regulatory requirements. Work is performed under the direct supervision of a pharmacist.

Responsibilities

• Accurately perform pharmaceutical calculations and prepare intravenous admixtures and any other tasks as required that relate to the dispensing of infusion therapy or as assigned
• Interact with professional staff and public on a daily basis
• Perform certain routine and repetitive functions and engage in sterile and non-sterile preparation and packaging of medications and other pharmacy related functions, under direct supervision of a Registered Pharmacist
• Maintain inventory control of pharmaceuticals
• May need to perform order entry of prescriptions into the outpatient pharmacy computer and assist in filling of new prescriptions or refills including cashiering
• Assist in training and orientation of pharmacy technicians, interns and pharmacists and be responsible for other duties as assigned

Qualifications

• Must have a current Washington State Pharmacy Technician License
• High school graduate or equivalent
• Able to work under direct supervision of a pharmacist in providing service to patients
• Able to communicate with other health care professionals, and the public in a polite and appropriate manner
• Must have proper aseptic technique experience in accurate, efficient and timely preparation of parenteral products
• Good oral and written communication skills
• Experience with computer systems and data entry
• Able to work independently in a creative and assertive manner
• Able to maintain patient confidentiality
• Able to perform basic pharmaceutical calculations
• Able to perform Pharmacy Technician functions including preparation, packaging and labeling of medication in an accurate and efficient manner

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The Program Manager is responsible for managing key internal and external activities determining program success, such as tracking deliverables, coordinating efforts, and identifying and managing critical program outcomes.

Responsibilities

• Work with the medical directors and other team members to develop overall program strategy, milestones and annual goals
• Partner with medical directors and other team members to determine program success and timing for strategic decision-making reviews throughout the program
• Work with medical directors and other team members to identify and proactively drive program deliverables and proactively manage program scope
• Develop and track detailed program plans including schedules, cost estimates, resource and communication plans
• Help to develop and maintain high-performing teams
• Work closely with resource team leaders to ensure appropriate allocation of resources to the program.
• Coordinate and contribute to the development of donor reports, along with partnering with the Fred Hutchinson Cancer Research Center’s Development Office
• Lead other staff team members including community health worker and patient navigator
• Contribute to the improvement of program management systems and tools
• Serve as a resource for questions related to program development and management processes

Qualifications

• Bachelor’s degree or higher, preferably a master’s degree in public health or health services
• Experience on project or program management, especially on community outreach, health education and/or tobacco cessation. Specifically, experience with American Indian/Alaskan Native community outreach would be a strength for this position.
• Extensive knowledge implementing and using project management systems and project reporting
• Ability to work effectively on fast-paced, complex projects
• Advanced computer skills, including MS Word, Excel, PowerPoint. Experience with SharePoint desired
• Strong interpersonal skills and ability to foster team work
• Excellent oral and written communication skills

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The BMT Intake Support Staff Supervisor is primarily responsible for the oversight of daily operational activities within the clinic and the staff teams working in the department. This includes the recruitment, training, and performance management of staff as well as daily operational performance and serving as a liaison with management and staff.

Responsibilities

• Participates in the recruitment process for new staff including the development and oversight of orientation
• Conducts staff performance management activities which includes evaluating and providing feedback on performance
• Develops staff training and participates in training delivery
• Oversees the daily work of the support staff, assists staff in prioritizing workloads when necessary, and ensures appropriate, daily staff coverage
• Encourages and fosters an environment of continuous performance improvement
• Serves a primary escalation point for troubleshooting and resolving issues surfaced by front line staff
• Communicates relevant information to both managers and frontline staff
• Oversees the development of policies and procedures
• Maintains a working knowledge of all support staff responsibilities and provides coverage as needed

Qualifications

Required:

• High School graduate or equivalent
• At least three years of relevant experience with a proven track record of increasing responsibility.
• Ability to manage sensitive situations with discretion
• Ability to demonstrate sensitivity and empathy in an emotionally challenging environment
• Ability to provide effective and timely feedback on staff performance
• Ability to communicate verbally in person, on the phone, and in writing in a clear, concise and professional manner
• Ability to apply active listening skills
• Ability to work in a high pressure, deadline oriented, and complex health care environment
• Ability to prioritize work assignments and adjust tasks as needed
• Ability to identify and triage issues appropriately
• Ability to collect and analyze data for performance and service metrics

Preferred:

• Preferred Associate or Bachelor's Degree
• Healthcare experience
• Proficient in utilizing an electronic medical record system
• Proficient in utilizing an electronic patient scheduling system
• Proficient in call distribution software (Intake/Imaging Scheduling/Information technology only)
• Familiarity with medical terminology

Overview

Seattle Cancer Care Alliance (SCCA) brings together the leading research teams and cancer specialists of Fred Hutch, Seattle Children’s, and UW Medicine. One extraordinary group whose sole mission is the pursuit of better, longer, richer lives for our patients. SCCA's purpose is to provide state-of-the-art, patient and family centered care; support the conduct of cancer clinical research and education; enhance access to improved cancer interventions; and advance the standard of cancer care regionally and beyond.

Every individual at SCCA plays a unique role in supporting our mission. Our collective success hinges on each of us conducting ourselves in accord with a set of core values:

• We are patient-centered. Everything we do must be linked to our ability to deliver better, safer outcomes for our patients.
• We are innovative. We nurture an environment that fosters unconventional thinking, a passion for discovery, and the open-mindedness to invite discovery from unexpected places.
• We are respectful. We are deeply respectful of our patients, their families, and each of our colleagues who serve them in so many different and important ways.
• We are collaborative. We understand that asking for and offering help in how to do better is not just a right, but among our most important responsibilities.
• We are agile. We cannot just be comfortable with change; we must embrace it as proof that we are making progress.
• We are responsible. Because our work is focused on people's well-being, we approach it with the highest level of ethical, fiduciary, and environmental responsibility.

This is an extraordinary opportunity to lead disruptive continuous innovations in the fight against cancer

Responsibilities

• Monitors and reviews assigned inventory levels by physical count, record keeping and/or visual inspection
• Enters inventory count data into the HEMM system
• Gathers required supplies from the storeroom inventory, and replenishes each inventory location as required.
• Document all inventory transactions as they occur, utilizing the HEMM system or department requisition clip board.
• Communicate inventory shortages to Supervisor or Buyer.
• Maintain requisitions or order manually or in automated system to track status of issues and requirements as necessary
• Checks storeroom for outdates and inventory to pull down. Checks shelves for kits to be made.
• Stores materials, supplies or equipment according to location, weight, size, safety or other requirements, marks stock shelves or bins with identifying codes, letters or figures.
• Assists with product order as it arrives each morning, i.e. putting away in storeroom, labeling patient chargeable product for clinic
• Rotates inventory to ensure FIFO standards
• Moves or transports items from stock to other areas using hand truck or other materials handling equipment
• Trains new workers in area operations.
• The typical shift will be 6AM-10AM

Qualifications

• A High School Degree, GED, or equivalent combination of education and experience from which comparable knowledge and abilities can be acquired is necessary
• One-year experience in supply logistics is necessary, with experience in a health care environment preferred.
• Knowledge of computerized or automated system operations
• Knowledge of record keeping practices
• Knowledge of safety practices
• Skill in lifting heavy packages and objects
• Must be able to push / pull cart with 400lb load, lift 50lb using proper technique
• Ability to effectively communicate

Overview

Seattle Cancer Care Alliance (SCCA) brings together the leading research teams and cancer specialists of Fred Hutch, Seattle Children’s, and UW Medicine. One extraordinary group whose sole mission is the pursuit of better, longer, richer lives for our patients. SCCA's purpose is to provide state-of-the-art, patient and family centered care; support the conduct of cancer clinical research and education; enhance access to improved cancer interventions; and advance the standard of cancer care regionally and beyond.

This job is responsible for routinely compounding and distributing medication and pharmaceutical supplies in both IV admixture and pharmacy distribution areas, in accordance with facility standards and procedures and regulatory requirements. Work is performed under the direct supervision of a pharmacist. Staffing in Investigational Drug Services Pharmacy is a rotation of this position.

Responsibilities

• Accurately perform pharmaceutical calculations and prepare intravenous admixtures and any other tasks as required that relate to the dispensing of infusion therapy or as assigned.
• Interact with professional staff and public on a daily basis.
• Perform certain routine and repetitive functions and engage in sterile and non-sterile preparation and packaging of medications and other pharmacy related functions, under direct supervision of a Registered Pharmacist.
• Maintain inventory control of pharmaceuticals.
• Assist in training and orientation of pharmacy technicians, interns and pharmacists and be responsible for other duties as assigned.
• May need to perform order entry of prescriptions into the outpatient pharmacy computer and assist in filling of new prescriptions or refills including cashiering.

Qualifications

• High school graduate or equivalent
• Must have a current Washington State Pharmacy Technician License.
• Able to work under direct supervision of a pharmacist in providing service to patients.
• Able to communicate with other health care professionals, and the public in a polite and appropriate manner.
• Must have proper aseptic technique experience in accurate, efficient and timely preparation of parenteral products.
• Good oral and written communication skills.
• Experience with computer systems and data entry.
• Able to work independently in a creative and assertive manner.
• Able to maintain patient confidentiality.
• Able to perform basic pharmaceutical calculations.
• Able to perform Pharmacy Technician functions including preparation, packaging and labeling of medication in an accurate and efficient manner.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

Responsibilities

The Parkhurst laboratory in the Basic Sciences Division is recruiting an hourly Lab Aide for 16-18 hours per week. The lab aide will coordinate with lab members and work a consistent weekly schedule (i.e., 2x 8hrs or 3x 6 hours) with some flexibility for shift days/times. Responsibilities include:

• Care and maintenance of fly stocks
• General lab maintenance, including preparation of lab reagents and stock solutions, cleaning, sterilizing labware, and other duties, as assigned.

Qualifications

• Graduation from High School or equivalent with interest in the sciences
• Must be reliable, able to produce consistent high quality results, and able to lift trays weighing 20-30 pounds
• Attention to detail is essential to this position
• Some lab experience and/or college level chemistry courses preferred

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

Responsibilities

The lab aide provides routine and specified support to assist a smooth daily operation in the Grady lab in a safe and proficient manner. The routine tasks may include preparation and mixing of solutions/reagents and keeping the laboratory tidy and organized. In addition, the incumbent may perform other duties and responsibilities (defrosting freezers; organizing cryotanks/freezers/fridge, annual pipette calibration) as instructed by lab manager.

Qualifications

• Currently enrolled in undergraduate study
• Minimum of 1 year experience in data entry
• Strong verbal and written communication skills 
• Strong computer skills and experience working with databases
• Minimum keyboard speed of 35 WPM 
• Experience in a job requiring attention to detail and accuracy

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

Responsibilities

The Lund Laboratory is recruiting a work-study student to assist with basic laboratory maintenance. This may include:

• Provide basic support to the laboratory
• Assist with murine colony
• Assist with genotyping/PCR
• Stock lab products
• Autoclave and remove biohazard trash
• Prepare reagents
• Perform general lab maintenance/upkeep
• Assist with set-up of experiments and work with biohazardous materials, HIV and HSV
• Perform other duties as assigned

Qualifications

Off-Campus Work Study authorization is required for this position. All students must provide a Financial Aid Award Letter or an Authorization to work off-campus to verify their eligibility if selected for this position.

• A high school diploma or GED is required.
• Currently enrolled in college.
• No previous experience is necessary.
• Knowledge of computer usage (especially use of spreadsheets and databases) is highly desirable.
• Accuracy and attention to detail is essential.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Brent lab is seeking undergraduate or graduate student to help with two ongoing projects. The ideal candidate will be available for 19 hours per week and be eligible for state or federal work study. Schedule can vary depending on class or other work schedule.

Ideal candidates would work independently and without much guidance from other lab members, should have successful experience making and manipulating DNA constructions, and in genetic manipulation of E. coli and/ or S. cerevisiae.

Responsibilities

• Carry out protocols such as PCR, yeast transformations, gel electrophoresis, etc.
• Be able to locate and retrieve specimens in response to investigator requests.
• Assist with lab and equipment maintenance.
• Assist with research projects as directed.

Qualifications

Required:

• Completion of a high school degree and work-study eligibility.
• The ideal candidate would be pursuing a graduate degree in Microbiology or Cell & Molecular Biology or a related field.
• Students with flexible schedules and a strong interest in microbiology/molecular biology.

Preferred:

• Strong computer skills using programs such as R or Python.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

This position is in a laboratory that uses molecular, genetic, and cellular techniques to explore the neural mechanisms that underlie the sense of smell and instinctive odor responses in mammals. One major lab focus is how thousands of diverse chemicals are perceived as having different odors. Another is how some chemicals elicit innate responses, such as attraction or aversion, or induce instinctive behaviors, such as fear.

Responsibilities

The individual in this position will be involved in projects exploring the neural pathways through which odor signals travel in the brain and/or how the organization of the olfactory system is established during development. The techniques likely to be used include tissue sectioning, immunohistochemistry, in situ hybridization, and microscope imaging. The incumbent will be responsible for tissue preparation and analysis methods, such as cryostat tissue sectioning and immunostaining. They will also be responsible for general laboratory duties, such as preparation of lab stock solutions, lab maintenance, autoclaving, and/or emptying biohazard waste. Major duties include:

• Prepare cryostat brain sections
• Conduct immunostaining and in situ hybridization of tissue sections
• Conduct microscope imaging and analysis of tissue staining
• Stock lab supplies, prepare reagents, autoclave and/or empty biohazard waste
• Follow safety/biohazard precautions and procedures

Qualifications

• A high school diploma or GED and enrollment in a university-level science degree program (e.g. biology, chemistry, or biochemistry) are required. Previous or current coursework in biology and/or chemistry and past laboratory experience are preferred
• Experience with molecular biology techniques is highly desirable
• Demonstrated accuracy, attention to detail, and ability to learn new skills quickly is essential
• This position requires work-study eligibility

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch's pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation's first cancer prevention research program, as well as the clinical coordinating center of the Women's Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

Responsibilities

The Malik lab in the Basic Sciences Division of Fred Hutch is looking to hire either a full-time or a part-time lab aide. This lab aide will assist researchers with fruit fly husbandry and stock room maintenance.  Responsibilities will also include media preparation for our bacterial and yeast related projects.  This could be an ideal position for sophomores or juniors who have completed intro to chemistry and are looking to get experience working in a lab, but we encourage anyone qualified to apply.

If a candidate needs part-time rather than full-time, they must be able to work at least a minimum of 16-18 hours per week, and to commit to the same schedule weekly.  However, preference is for someone at higher part-time hours (25/wk) or full-time.

Qualifications

• Completion of a high school degree is required
• Must have completed college level coursework in Biology. Past experience in genetics and/or fruit fly husbandry is desirable.
• Must have careful attention to detail and a reliable schedule for fixed hours every week.

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Statistical Center for HIV/AIDS Research and Prevention (SCHARP) at Fred Hutch is a full service statistical and data management center focused on HIV prevention research. SCHARP has an annual budget of over $40 million, more than 180 employees and is currently managing over 40 active phase I – III clinical trials in over 150 clinical sites around the world. SCHARP is seeking a Lab Data Coordinator. The Lab Data Coordinator (LDC) monitors the collection and processing of and performs routine data entry and quality control of laboratory specimen and assay data pipelines at the Statistical Center for HIV/AIDS Research and Prevention (SCHARP). The LDC will work within a network/study/research protocol team to support the policies and goals of each project assigned study or project. She/He will develop and maintain successful working relationships with protocol their teams and specific research sites to ensure and maintain data integrity and quality.

Responsibilities

The Lab Data Coordinator will be part of a team of data coordinators and data managers who work closely with programmers to oversee all SCHARP laboratory data pipelines. The incumbent will work under the supervision of the Lab Data Management leadership and the mentorship of the Sr. Lab Data Coordinators and lab data managers. She/he will refer all non-routine decisions for the management of data to study/protocol leads and/or departmental leadership.

Responsibilities may include:

• Attend study team meetings and conference calls and with guidance, serve as a LDM representative.
• Serve as a liaison between SCHARP study teams and external collaborators to establish and monitor specimen data pipelines and assay data from clinical trials and associated specimen repositories.
• Oversee and distribute standardized specimen data discrepancy reports.
• Work with external labs, SCHARP lab programmers and clinical data managers to investigate and resolve data discrepancies and troubleshoot issues as needed.
• Identify opportunities for process improvements and collaborate to develop and implement solutions.
• Work with SCHARP lab data managers, specialists and programmers to develop specifications / requirements for lab data management processing and quality control systems
• Act as a liaison between the SCHARP lab data management unit and clinical research sites or external labs; and with supervision represent LDM on SCHARP study teams and in internal and external meetings.
• Help maintain lab, assay and specimen metadata.
• Respond to and resolves quality control queries from labs.
• Provide operational support to labs for tools that SCHARP maintains and operates, including Atlas and custom SCHARP tools.
• With supervision, develop Data Transfer Plans (DTPs) and other documentation associated with specimen and assay data transfers.
• Escalate issues to the Lab Data Management leadership as needed.
• Adhere to quality assurance procedures, standard operating procedures, and work practice guidelines and support documentation of these efforts.

Qualifications

Minimum Qualifications

• Bachelor’s degree in biological sciences, or equivalent
• Minimum 2 years of clinical or lab data management experience
• Demonstrated ability to work independently and as part of a team
• Demonstrated ability to manage multiple projects and competing priorities
• Must be flexible, work well in a team environment, and be capable of meeting tight deadlines
• Must be organized and detail-oriented, with excellent oral and written communication skills

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

About the department

The Pharmacokinetics Laboratory at SCCA is specialized in Therapeutic Drug Monitoring (TDM) for patients diagnosed with various blood disorders. The laboratory provides its expertise and support to many providers who seek to improve their patient’s transplant outcomes. Providing clinical services for more than 15 years, it is one of the most highly regarded laboratories in the medical community and has clients across USA and Canada.

Responsibilities

The main responsibilities are described below:

1. Be accessible to the laboratory staff during normal operating hours as scheduled to provide onsite, telephone, and/or electronic consultation to laboratory staff and clients for busulfan therapeutic drug monitoring.
2. Review busulfan pharmacokinetics data and dose recommendations. Be available for consultation to laboratory clients on matters relating to the quality of the test results and their interpretation concerning specific patient populations.
3. Work with Laboratory Manager and Director in monitoring quality control to ensure high quality, accurate results.
4. Work with SCCA/UW Pharmacy and other back-up resources to be scheduled for PK data review, dose recommendations, and consultation.

Qualifications

• PharmD, PhD, or MD with at least one year of clinically applicable pharmacokinetics/pharmacodynamics experience is required
• Must be licensed in the State of Washington and have appropriate board certification
• Previous oncology, pharmacology, pharmacogenetics and/or pharmacokinetics experience is required.
• Excellent communication, both written and verbal
• Strict attention to detail
• Strong math and computer skills, including ability to create and interpret data
• Multi-task oriented—ability to prioritize and drive multiple initiatives
• Ability to work in a rapidly changing environment
• Ability to implement directions provided by management

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. The Center’s five scientific divisions collaborate to form a unique environment for conducting basic and applied science. Vaccine and Infectious Diseases Division (VIDD) works to eliminate or minimize the impact of globally significant infectious diseases. Within VIDD is the Statistical Center for HIV/AIDS Research & Prevention (SCHARP), which provides statistical support and data management to researchers worldwide in the fight against HIV/AIDS with active studies in the U.S., Africa, Latin America, Asia and Europe. Careers Start Here.

The Statistical Center for HIV/AIDS Research and Prevention (SCHARP) at Fred Hutch is a full service statistical and data management center focused on HIV prevention research. SCHARP has an annual budget of over $40 million, more than 180 employees and is currently managing over 40 active phase I – III clinical trials in over 150 clinical sites around the world. SCHARP is seeking is seeking a Lead Data Standards Analst. Under minimal supervision, the Lead Data Standards Analyst oversees the coordination and management of clinical data standards and production of standard datasets within SCHARP. The incumbent provides subject matter expertise in CDISC data standards, leads coordination efforts with SCHARP staff and network partners to standardize the collection and tabulation of clinical trials data, chairs the Data Standards Committee to govern CRF alignment with CDASH and change control for SCHARP SDTM and ADaM specifications, trains others in CDISC standards and SCHARP dataset configurations, reviews and approves draft SDTM and ADaM metadata and conversion specifications prior to implementation, configures data transformations to provision SCHARP SDTM data tables from CRF and other data pipelines to SCHARP Programmers and Statistical Research Associates via a clinical data warehouse, and may supervise Data Standards Analysts in support of above described activities.

Core to the role is a deep understanding of data standards and data transformations, the ability to communicate effectively, work collaboratively with colleagues and be responsive to the needs of both internal and external customers within an environment of mutual cooperation and respect.

Responsibilities

• The Lead Data Standards Analyst ensures that SCHARP studies produce high-quality CDISC datasets aligned with SCHARP standards and compliant with the latest published electronic regulatory submissions standards including:
  • CDISC Clinical Data Acquisition Standards Harmonization (CDASH), Study Data Tabulation Model (SDTM), Analysis Data Model (ADaM), and Define-XML.
  • Controlled Terminology (CT) published by CDISC and NCI, as well as SCHARP-defined terminology
  • Electronic Common Technical Document (eCTD), Study Data Standards Documents, and other electronic submissions guidance issued by drug and medical device governing authorities.
• As Chair of the Data Standards Committee, governs the process for maintaining organizational data standards for clinical data collection, management, and reporting.
• Reviews and approves the draft of SDTM and ADaM metadata and conversion specifications prior to the implementation of these specifications in the clinical data warehouse.
• Configures data transformations to provision SCHARP SDTM data tables from CRF and other data pipelines to SCHARP Programmers and Statistical Research Associates via a clinical data warehouse.
• Provides oversight to the SCHARP SDTM and ADaM data specifications – the operating clinical data models used for reporting and deriving clinical datasets and analysis datasets, respectively.
• Stays informed of updates to CDISC data specifications; incorporates new versions of SDTM into SCHARP SDTM and advises to others in SCHARP on CDASH and ADaM.
• Works with study teams to lead the definition and documentation of per study SDTM metadata and conversion specifications and ensures alignment with organizational data standards.
• Provides study teams with insight to the SCHARP ADaM data specifications.
• Defines and documents per study clinical data transformations to SDTM+- from data collection formats such as CDASH.
• Implements clinical data transformations of source data to SCHARP SDTM using database ETL tools. Specifies complex transformations and consults with Programmers, as needed, to implement.
• Reviews and validates derived SCHARP SDTM and ADaM datasets using Pinnacle 21 to ensure compliance with published specifications and industry and regulatory requirements.
• Works with IT to identify and recommend enhancements to the database ETL toolset.
• Coordinates and may provide internal CDISC training to SCHARP and our partners as appropriate.
• Provides supervision and leadership by training and mentoring others involved with CDISC standards, SCHARP dataset configurations, and regulatory and/or sponsor specific data requirements.

Qualifications

Minimum qualifications

• Bachelor’s degree in Library Sciences, Informatics, Information Systems, Computer Science or other relative discipline
• Five years of industry experience developing and implementing CDISC data standards
• Working knowledge of CDASH, SDTM and ADaM
• Excellent written and verbal communication skills, with the ability to work well in multi-faceted teams
• Experience working with data documentation formats such as CSV, JSON, and XML
• Expertise using Microsoft Excel

Preferred qualifications

• Experience building transformation pipelines using modern ETL tools such as IBM InfoSphere DataStage, Pentaho/Kettle, SQL Server Integration Services, or other
• Experience supervising or mentoring others
• Experience programming with a modern procedural, declarative, or statistical programming language such as SAS, Perl, Python, Shell or SQL
• Experience working in an environment governed by Good Clinical Practices, Good Clinical Data Management Practices, or other FDA guidelines
• Experience with Electronic Data Capture (EDC) systems

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

As a Site Reliability Engineer, you will be responsible for developing and managing cloud server infrastructure and networks, monitoring and improving system performance, building and maintaining CI/CD systems that facilitate build automation and automated testing, and help formulate and implement security policies. You will work with operations, support and engineering teams to ensure the automation platform is capable of serving current and future needs. You will document and drive best-practices across the team.

The ideal candidate is proficient in coding, thinks in terms of architecture and test automation, and has substantive experience writing code running within a changing environment where servers and databases are interchangeable and impermanent. Candidates should have the ability to take existing application and refactor, redesign with modern solutions (such as containizing existing monolithic applications). Have a strong desire to pursue the principles of infrastructure as code, holistic infrastructure design, immutable infrastructure, and orchestration and automation whenever possible.

Responsibilities

• Develop automations to manage the infrastructure.
• Research/analyze data processing functions, methods and procedures.
• Monitor production systems for expected performance.
• Perform root cause analysis on production issues and determine action items for prevention and resolution.
• Participate in architectural decisions about the next iterations of our cloud environments.

Qualifications

• Experience working with AWS (ECS/Fargate is required)
• Strong knowledge of infrastructure tools (CloudFormation or Terraform)
• Strong knowledge with one or more configuration management tools (Ansible is preferred)
• Experience with Docker
• Strong knowledge with one or more build automation tool (Gitlab is preferred)
• Experience with application and systems monitoring services and logging solutions (Splunk and Datadog are preferred)
• Linux systems support in a 24x7 production environment.
• Ability to manage multiple activities and changing priorities
• 3-5 years of experience in enterprise level IT projects Cloud based technologies (PaaS, IaaS, Cloud Infrastructure Services)

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

The Statistical Center for HIV/AIDS Research and Prevention (SCHARP) at Fred Hutch is a full service statistical and data management center focused on HIV prevention research. SCHARP has an annual budget of over $40 million, more than 180 employees and is currently managing over 40 active phase I – III clinical trials in over 150 clinical sites around the world. SCHARP is seeking a Lead Software Developer with professional experience to add to our development team.

Responsibilities

• Lead development teams and facilitate design decisions 
• Create and maintain technical specifications and architecture documents 
• Implement and maintain systems within a validated software development lifecycle 
• Participate in agile requirements gathering, design and tasking 
• Provide operational support for existing systems 
• Work on a project team with customers, business analysts, project management and testers 
• Work on a development team creating and following standards that help with cross training and reducing system maintenance tails 

Qualifications

Minimum: 

• 5+ years professional experience in software development 
• Expertise with modern OOP programming paradigms / languages 
• Experience with relational data modeling: conceptual and physical 
• Defining and writing automated unit and functional tests 
• Detail oriented including the following: 
  • Ability to understand a system of complex interactions
  • Capable of deep troubleshooting and discovering root causes of problems
  • Writes unit tests with the same care as product code
  • Has well-commented code 

Preferred: 

• Java full stack web application development experience, both front-end and back-end 
• Agile development 
• UNIX systems 
• PostgreSQL 
• Javascript, Selenium 
• Play Framework 
• Microservice architecture 
• Docker, Kubernetes, AWS 
• Functional programming
• Working in a regulated environment such as 21 CFR Part 11, Sarbanes-Oxley or HIPPA 

Culture: 

• Work in an organization that strives to make the world a better place.  
• Work with developers who enjoy crafting quality code and robust performant systems.  
• Work in vibrant South Lake Union Seattle.  
• Strong commitment from management to a 40 hour work week.  
• Benefits include paid vacation, holidays, sick time, medical, dental and vision benefits as well as 403 (b) retirement plan. 

Overview

Click HERE to apply for Licensed Practical Nurse (LPN)

The Licensed Practical Nurse (LPN) functions under the supervision and guidance of the clinical nurse, nursing supervisor, or physician and participates in the multi-disciplinary process of providing care and treatment to patients and provides clinical support and technical assistance to the professional medical and other staff.

The LPN is responsible for functioning within the scope of practice dictated by the authority of Washington State Department of Health and functions in an interdependent role to deliver care as directed and assists in the revision of care plan in collaboration with the registered nurse. The LPN functions in a dependent role when executing a medical regimen under the directions and supervision of an advanced nurse practitioner, licensed physician, and/or physician assistant. An LPN may not accept delegation of acts not within their scope of practice. Individual must be able to manage demanding workload with accuracy. Position requires excellent customer service skills with patients, and their families, other staff, physicians, vendors, and the public.

Responsibilities

Click HERE to apply for Licensed Practical Nurse (LPN)

• Assists with consultations and follow-up visits, including putting patients in rooms, interviewing patients, recording vital signs including pulse rate, blood pressure, height and weight, and enters information in patient electronic medical record.
• Performs select clinical tests including, but not limited to; urinalysis, urine bun/creatinine, pregnancy tests, and blood glucose monitoring. Manages and operates equipment safely and correctly.
• Administers and documents medication under physician’s order and follows the five (5) mediation rights and reduces the potential for medical error.
• Provides direct patient care to pediatric and adult population
• Performs venipuncture, accesses implanted ports and maintains central venous devices.
• Assesses patient and family needs and provides ongoing education on radiation therapy, plan of care, symptom management.
• Assists providers with equipment and procedures.
• Checks and appropriately knows how to clean head and neck chairs, scope, laryngoscope
• Adheres to ANA Nursing Scope of Practice
• Triages patient and family phone calls and reports relevant information to primary nurse, providers. In addition, documents information in Electronic Medical Records (EMR)
• Maintains patient confidentiality and HIPAA regulations.

Qualifications

Click HERE to apply for Licensed Practical Nurse (LPN)

• One year experience in patient care required
• Two years of oncology experience preferred
• Demonstrate responsibility and accountability for professional practice, continues growth and self-evaluation
• Adhere to employer work practices as described in the Employee Handbook and SPTC policies and procedures
• Document work processes as required
• Maintain professional appearance and personal conduct at tall times
• Effectively cope with typical job stress
• Perform other duties assigned.
• Strong organizational and interpersonal skills
• Ability to use various types of equipment for examination and treatment procedures.
• Ability to maintain quality control standards.
• Ability to identify problems and recommend solutions
• Current State of Washington LPN licensure
• Certification in Basic Life Support (BLS) Required

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The Licensed Practical Nurse (LPN) assists in the delivery of patient care under the direction and supervision of the site supervisor/manager. The LPN contributes to the assessment of a patient's care, assists in the development of a plan of care, implements aspects of care as directed, and participates in evaluating care.

Responsibilities

• Performs limited assessment of patients
• Records and reports patient's condition and reaction to drugs and treatments to the RN and/or MD/ARN
• Administers medications, injections and vaccines as ordered by a licensed provider and within LPN scope of practice and SCCA policy
• Educates patients, families, and caregivers, answers their questions, and appropriately refers their clinical care questions to the clinical care team
• Additionally, a LPN may:
  • Perform basic phlebotomy, IV insertion, accessing central venous catheters, and basic management of central venous catheter dressings IAW SCCA Policies and Procedures
  • Perform basic management and accessing port-a-cath (implanted port) in accordance with established SCCA Policies and Procedures
  • Collects, handles, and labels specimens in accordance with established SCCA Policies and Procedures
  • Be a team member in the Code Response Team

Qualifications

Required:

• Degree or program that provides the eligibility to attain certification and/or licensure
• Current Washington State nursing license
• Current BLS AHA Health Provider Card (or equivalent course, such as by the American Red Cross) and renewal required every two years
• Ability to observe and record patient’s symptoms or signs of distress and respond appropriately to those symptoms
• Ability to organize and manage time and tasks independently
• Ability to communicate verbally in person, on the phone, and in writing in a clear, concise and professional manner
• Proficient with email software systems
• Ability to work in a high pressure, time-sensitive, and complex health care environment
• Ability to practice the critical thinking skills of analyzing, applying standards, discriminating, information seeking, logical reasoning, predicting, and transforming knowledge

Preferred:

• One year or greater of LPN practice in an oncology and/or ambulatory setting
• Experience with Electronic Medical Records
• Basic understanding of proper labeling and management of specimens

Overview

Cures Start Here. At Fred Hutchinson Cancer Research Center, home to three Nobel laureates, interdisciplinary teams of world-renowned scientists seek new and innovative ways to prevent, diagnose and treat cancer, HIV/AIDS and other life-threatening diseases. Fred Hutch’s pioneering work in bone marrow transplantation led to the development of immunotherapy, which harnesses the power of the immune system to treat cancer. An independent, nonprofit research institute based in Seattle, Fred Hutch houses the nation’s first cancer prevention research program, as well as the clinical coordinating center of the Women’s Health Initiative and the international headquarters of the HIV Vaccine Trials Network. Careers Start Here.

This position supports the Mech/Arch, Controls, and PM teams of the Facilities Engineering department by supporting the Leads and Supervisors in any area they require help in as approved by the Operations Supervisor, by coordinating and balancing PM workload between all three teams and all three shifts, by managing the 20 year plan including providing replacement analysis of various pieces of equipment on their replacement year and identifying new pieces of equipment and systems to include in the plan, by establishing SOPs for various work task and PMs within the department and in particular when a new piece of equipment is added researching and quantifying the PM’s needed in conjunction with the Lead and Supervisor in that area, by coordinating outages both with the workforce and the customers, by providing long range forecast of anticipated workload, and by providing detailed estimates for all customer Work Orders greater than 8 hours. Additionally, the individual will process and close all PMs in their related areas, QCing at least 10% of the PMs to ensure proper completion, Ensuring clear equipment histories are developed and maintained, and that proper costs are associated to PMs and projects. This individual will also be the technical manager of many small contracts in their area of responsibility and will perform analysis and studies as directed.

Responsibilities

• Uses the CMMS database to plan, schedule, and coordinate the preventive maintenance of mechanical equipment, including A/C units, air compressors, boilers, chillers, air handlers, etc. 
• New work orders (CM, CR and TC) will be processed by Supervisors/Leads. Prioritize, plan, schedule and follow – up on accuracy of the job plan for all planned (PM, corrective) work.
• Their focus is not day to day but is to be proactive and optimize workforce productivity and minimize plant downtime by managing work 2 weeks to 1 month in advance.
• Providing reports to supervisors and leads on schedule compliance:
  • Jobs worked and completed as scheduled, planning compliance
  • Accuracy of information, estimate of labor and material, and improvement in labor effectiveness or increase of value added activities
  • Work sampling, etc.
• Develops, incorporates and implements and trains personnel in preventive maintenance plans / SOPs and schedules for all facilities related equipment into the CMMS system.
• Modifies database to add/remove equipment, develop and modify job plans, modify maintenance intervals and identifies special requirements for maintenance of technical facilities.
• Ensures records for documentation of completed work, compliance with regulations and certification requirements are maintained. 
• Provide customer requested estimates for work for in house staff and outside contractors.
• Coordinates with outside contractors and informs building administration on all equipment, and utility shutdowns. 
• Update and maintain the 20 year plan for equipment and infrastructure for the Center by conducting analysis of data.
• Prepares reports and recommends changes to improve performance of the 20 year plan. 
• Reviews design documents (internally and externally developed) for equipment standardization and incorporation into the CMMS.
• Ensures close-out documentation for all new equipment on new construction and renewal projects have been captured by CMMS and other campus databases.
• Maintains O&M Manuals (bound and electronic) as well as OEM Technical Data to support maintenance and repair activities.

Qualifications

• Bachelors degree or equivalent work experience and training
• At least 5 years' experience in facilities and or facilities maintenance
• Knowledge of computerized maintenance management systems (maintenance planning/scheduling software)
• Strong technical knowledge and practical experience in areas of Mechanical, Architectural, and HVAC operations and maintenance.
• Excellent organizational, communication and interpersonal skills with ability to interact independently with staff at all levels, cross-functional teams, and external entities
• Physical skills necessary to climb, bend, stoop, lift and perform tasks utilizing ladders and scaffolds, etc.
• Dependable, on-time and proven good work habits
• Able to work a varied schedule including shift work
• Ability to be an effective trainer
• Possess and maintain a valid Washington State Driver’s License

Overview

The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.

The Mammography Technologist performs mammographic procedures across all clinical sites, including the mobile mammography van, according to department procedure manual utilizing correct anatomic positioning, selects correct technical factors that consistently produce high quality mammogram images while considering patient variation and minimizing radiation.

Responsibilities

• Manages electronic data, processes information (subtraction or other digital manipulation) for interpretation, reviews exam for proper positioning, technique, identification, and records required information
• Transfer images to PACS and verifies the action. Reviews the case, patient medical history, protocol, and prior images, using clinical judgement to ensure a successful outcome
• Instructs radiology students and/or new staff according to clinical and department requirements; assists in the orientation of department and hospital personnel with emphasis on radiation safety
• Performs visual maintenance and quality controls checks, records and reports results to appropriate personnel, identifies problems and communicates them to immediate supervisor, takes appropriate corrective action when necessary, and offers solutions as appropriate
• Responsible for ensuring an adequate inventory of supplies, linens, and accessories
• Coordinates and schedules examinations

Qualifications

Required:

• Degree or program that provides you the eligibility to attain certification or licensure
• Washington State Radiologic Technologist Certification
• Completed 8 hours of training in using a mammographic modality (e.g., digital), before beginning to use that modality independently
• Meets one of the following:
  • A. If Qualified BEFORE April 28,1999, must be certified by:American Registry of Radiologic Technologists (ARRT) OR - American Registry of Clinical Radiologic Technologists, OR - Licensed to perform general radiographic procedures in a state AND 40 hours of training in mammography
  • B. If Qualified AFTER April 28,1999, must be certified by American Registry of Radiologic Technologists (ARRT), American Registry of Clinical Radiologic Technologists, or, Licensed to perform general radiographic procedures in a state. Additionally, completed 40 hours of training in mammography including training in breast anatomy and physiology, positioning and compression, QA/QC techniques, and imaging of patients with breast implants and completed 25 mammography examinations under direct supervision of an appropriate MQSA-qualified individual
  • C. If not registered, will become registered at first eligibility
• Ability to communicate verbally in person, on the phone, and in writing in a clear, concise and professional manner
• Ability to work independently, organize, and prioritize concurrent responsibilities and demands
• Ability to assess patients' conditions and request assistance when necessary
• Ability to assist in the movement of patient to and from wheelchairs, carts and radiographic tables.

Preferred:

• One year of mammography technologist experience
• Proficient in email and word processing systems
• Experience with Electronic Medical Records

Overview

Seattle Cancer Care Alliance brings together the leading research teams and cancer specialists of Fred Hutch, Seattle Children's, and UW Medicine. One extraordinary group whose sole mission is the pursuit of better, longer, richer lives for our patients.

Performs screening and diagnostic mammographic procedures on a per diem basis across all clinical sites, including mobile mammography van, in accordance with the American College of Radiology (ACR) guidelines at a technical level not requiring constant supervision; uses independent judgment to accomplish the efficient completion of prescribed procedures utilizing good patient care and proper radiation protection standards; assures correct film and file documentation; records information related to exams into department computer.

Responsibilities

Qualifications

All radiologic technologists performing mammography must meet the MQSA-required qualifications in the table below. The ACR also recommends that technologists performing mammography hold the American Registry of Radiologic Technologists (ARRT) post-primary certification in mammography.