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Clinical Research Coordinator I
Job Description
Overview:
This position would offer a variety in studies that we conduct as well as the various phases of study development. Benaroya Research Institute and the Clinical Trials Unit encourage teamwork and collaboration. We have unparalleled support from our physicians, clinic staff and study staff.
Responsibilities:
Subject care requirements may include:
The CRC I may also perform phlebotomy, specimen processing using universal precautions when appropriate and consistent with licensure; and participate in process improvement events as necessary. The CRC must maintain subject and document confidentiality at all times, understand and comply with the appropriate sponsor requirements, regulations including the Food and Drug Administration (FDA), Good Clinical Practice (GCP) and International Conference on Harmonization (ICH), Health Insurance Portability and Accountability Act (HIPAA), Institutional Review Boards, (IRB) and institutional policies and procedures.
Qualifications:
Visit BenaroyaResearch.org or follow BRI’s Autoimmune Life Blog, Facebook, Instagram,
LinkedIn or X to learn more.
The Clinical Research Coordinator I (CRC) performs increasingly complex tasks to facilitate clinical research, while providing service to Virginia Mason Physicians on their clinical trials specializing in Cardiology, Asthma/Allergy, Rheumatology, and Neurology. Strong communication and organization skills are required.
This position would offer a variety in studies that we conduct as well as the various phases of study development. Benaroya Research Institute and the Clinical Trials Unit encourage teamwork and collaboration. We have unparalleled support from our physicians, clinic staff and study staff.
- New study preparation
- Assistance with and input on investigator initiated protocol development
- Development of operating manuals and standard procedures for grant studies
- Subject screening and recruitment
- Informed consent
- Subject history
- Adverse events
- Concomitant medication review
- Regulatory document filing
- Preparation for study monitor visits
- TA handling
- Completion of case report forms
- Maintenance and development of source documents
- Eligibility verification
- Proper standard of research billing
- Ensuring site quality
Subject care requirements may include:
- Appointment scheduling
- Arriving
- Records review
- Treatment coordination
Collecting vital signs - Subject health assessment
- Telephone triage/screening
- At all times the CRC will ensure protocol compliance and subject safety
The CRC I may also perform phlebotomy, specimen processing using universal precautions when appropriate and consistent with licensure; and participate in process improvement events as necessary. The CRC must maintain subject and document confidentiality at all times, understand and comply with the appropriate sponsor requirements, regulations including the Food and Drug Administration (FDA), Good Clinical Practice (GCP) and International Conference on Harmonization (ICH), Health Insurance Portability and Accountability Act (HIPAA), Institutional Review Boards, (IRB) and institutional policies and procedures.
- Minimum one year full-time related experience within clinical research
- Prefer higher education or vocational training specializing in healthcare
- Requires good medical knowledge including medical terminology, and basic subject care
- May require Healthcare Licensure or other specialized training
- May require phlebotomy and vital sign collection skills and the ability to operate centrifuges and EKG machines
$22.70 to $32.92 per hour
Benefits:
- Medical, dental, vision hardware insurance
- Flexible spending accounts: health care, dependent care, commuter
- Short and long-term disability and life and AD&D insurance
- 403(b) retirement plan with matching funds after one year of employment
- PTO: 13 holidays, three weeks of vacation and two weeks of sick leave per year
- Employee assistance program
- Educational Assistance Program
- Subsidized bus pass
- YMCA rebate and other fitness club discounts
- Voluntary benefits, e.g., pet insurance, accident, critical illness, identify theft
- See benaroyaresearch.org for benefit details
The Clinical Research Program at the Benaroya Research Institute at Virginia Mason (BRI) is committed to giving patients access to clinical trials. Working with clinicians at Virginia Mason Franciscan Health (VMFH), the Clinical Research Program at BRI differentiates itself by focusing on patient-centered research. BRI is an independent, non-profit organization with a culture based on the values of collaboration, respect, innovation and inquiry. Team members work together to support patients and clinicians with the goal of better outcomes for all.
Visit BenaroyaResearch.org or follow BRI’s Autoimmune Life Blog, Facebook, Instagram,
LinkedIn or X to learn more.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, disability or protected veteran status. If you need assistance completing the application process, please contact Human Resources at 206-287-5646 or email jobs@benaroyaresearch.org
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