Clinical Research Coordinator III
Seattle, WA 
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Posted 14 days ago
Job Description
Clinical Research Coordinator III
Job ID 27492 Type Regular Full-Time Location US-WA-Seattle Category Clinical Research Support Services
Overview

Fred Hutchinson Cancer Center is an independent, nonprofit organization providing adult cancer treatment and groundbreaking research focused on cancer and infectious diseases. Based in Seattle, Fred Hutch is the only National Cancer Institute-designated cancer center in Washington.


With a track record of global leadership in bone marrow transplantation, HIV/AIDS prevention, immunotherapy and COVID-19 vaccines, Fred Hutch has earned a reputation as one of the world's leading cancer, infectious disease and biomedical research centers. Fred Hutch operates eight clinical care sites that provide medical oncology, infusion, radiation, proton therapy and related services, and network affiliations with hospitals in five states. Together, our fully integrated research and clinical care teams seek to discover new cures to the world's deadliest diseases and make life beyond cancer a reality.


At Fred Hutch we value collaboration, compassion, determination, excellence, innovation, integrity and respect. These values are grounded in and expressed through the principles of diversity, equity and inclusion. Our mission is directly tied to the humanity, dignity and inherent value of each employee, patient, community member and supporter. Our commitment to learning across our differences and similarities make us stronger. We seek employees who bring different and innovative ways of seeing the world and solving problems. Fred Hutch is in pursuit of becoming an anti-racist organization. We are committed to ensuring that all candidates hired share our commitment to diversity, anti-racism and inclusion.

The Clinical Research Coordinator III will work directly with hospital, clinic and research staff in the development, implementation and management of clinical trials.

Responsible for the collection, coordination, processing, and quality control of clinical trial data in accordance with protocols subject to FDA oversight. They are responsible for coordination of long-term follow-up activities associated with these protocols.

Te incumbent will use judgment in data collection, quality control, liaison, and research coordination activities. They will interact with patients, physicians, and other clinical providers and support staff within and outside of the Fred Hutch/Seattle Childrens UW system including the Fred Hutch Transplant Service.

This role will have the opportunity to work partially at our campus and remotely.

Responsibilities

This individual will work under limited supervision of the Clinical Research Operations Manager and will be required to perform their responsibilities with a high level of independence within the scope of study protocol(s) and institutional policies and guidelines.

    Review and maintain familiarity with research protocols with regard to data collection.
  • Research, maintain, analyze, and abstract patient clinical trial data from pre-study background (e.g., previous diagnoses and treatments) through clinical trial participation and long-term follow-up.
  • Evaluate patient eligibility for clinical trials and assist in screening and patient enrollment.
  • Understand and interact with departments and automated systems throughout Fred Hutch/Seattle Childrens/UW system to ensure timely and complete delivery of data.
  • Track status of potential and active clinical trial participants.
  • Manage long-term follow-up evaluations and data collection with clinical trial participants, Fred Hutch/Seattle Childrens, and participants' local physicians.
  • Develop data acquisition forms and instructions for completion.
  • Manage and work with computer application specialists to ensure consistency between paper and electronic data systems.
  • Manage monitoring visits and quality control reviews by Sponsors or Investigators.
  • Support regularly scheduled institutional monitoring visits by Sponsors or Investigators to ensure quality and completeness of data.
  • Serve as a liaison and reference resource to Physicians, Investigators, other staff members, and other organizations with questions about data collection or protocol procedures and requirements.
  • Manage special projects regarding data collection, analysis, output, and presentation.
  • Provide input to support policies and goals of the program. Manage submission of reports in conjunction with the PI and Sr. Clinical Research Manager to the Human Subjects Committee, Institutional Review Board, Radiation Safety Committee, Federal Drug Administration, Pharmaceutical Companies, and other agencies.
  • Liaise with Institutional Review Boards (IRB's) in submission of protocol, study amendments, annual reporting and adverse event reporting.
  • Assist with orientation and training of new staff.
  • Perform other responsibilities as required.
Qualifications

MINIMUM QUALIFICATIONS:

  • Bachelor's Degree in scientific/medical field or equivalent combination of education and experience.
  • Six or more years of experience in medical records, cancer registry, clinical study coordination or related field.
  • Strong verbal and written communication skills.
  • Knowledge of medical terminology.

PREFERRED QUALIFICATIONS:

  • Advanced Degree (Master's level or higher) in the scientific/medical field.
  • Clinical Research (CRA) certification is highly desirable
  • Strong computer skills, including proficiency in Excel and Word, and experience working with databases.

A statement describing your commitment and contributions toward greater diversity, equity, inclusion, and antiracism in your career or that will be made through your work at Fred Hutch is requested of all finalists.

The annual base salary range for this position is from $72,946 to $109,408, and pay offered will be based on experience and qualifications.

Fred Hutchinson Cancer Center offers employees a comprehensive benefits package designed to enhance health, well-being, and financial security. Benefits include medical/vision, dental, flexible spending accounts, life, disability, retirement, family life support, employee assistance program, onsite health clinic, tuition reimbursement, paid vacation (12-22 days per year), paid sick leave (12-25 days per year), paid holidays (13 days per year), paid parental leave (up to 4 weeks), and partially paid sabbatical leave (up to 6 months).

Our Commitment to Diversity
We are proud to be an Equal Employment Opportunity (EEO) and Vietnam Era Veterans Readjustment Assistance Act (VEVRAA) Employer. We are committed to cultivating a workplace in which diverse perspectives and experiences are welcomed and respected. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, sex, age, disability (physical or mental), marital or veteran status, genetic information, sexual orientation, gender identity, political ideology, or membership in any other legally protected class. We are an Affirmative Action employer. We encourage individuals with diverse backgrounds to apply and desire priority referrals of protected veterans. If due to a disability you need assistance/and or a reasonable accommodation during the application or recruiting process, please send a request to Human Resources at hrops@fredhutch.org or by calling 206-667-4700.

 

Job Summary
Start Date
As soon as possible
Employment Term and Type
Regular, Full Time
Required Education
Bachelor's Degree
Required Experience
6+ years
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