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Clinical Research Coordinator I​/II

Job in Seattle, King County, Washington, 98127, USA
Listing for: Benaroya Research Institute
Full Time position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 28.85 - 42.98 USD Hourly USD 28.85 42.98 HOUR
Job Description & How to Apply Below

Join a collaborative team at the Clinical Trials Unit of Benaroya Research Institute (BRI), where your work will directly support cutting‑edge clinical research in partnership with Virginia Mason physicians. Our studies focus on a variety of specialties including Cardiology (treatment of either new medications or cardiac devices), Neurology, and Allergy studies. This role offers exposure to a wide range of clinical trials across various phases of development.

You will be part of a supportive, team‑oriented environment with unparalleled support from our physicians, clinic staff, and dedicated study teams. We are seeking a motivated and detail‑oriented Clinical Research Coordinator (CRC) to support our Principal Investigators in executing high‑quality research protocols.

Schedule:

Typically Monday through Friday from 8:00 AM to 4:30 PM, with a 30‑minute lunch break. Work schedule may vary.

Responsibilities
  • Facilitate clinical research, including collaboration with affiliate or partnering research sites and conducting BRI‑based studies
  • Prepare for new studies, including regulatory document filing and study monitor visit preparation
  • Screen and recruit study subjects, obtain informed consent, and document subject history
  • Review adverse events, concomitant medications, and ensure protocol compliance and subject safety
  • Handle test articles (TA), complete case report forms, and maintain source documents
  • Manage proper standard or research billing and ensure site quality
  • Coordinate subject care, including appointment scheduling, record reviews, treatment coordination, and health assessments
  • Collect vital signs, perform telephone triage/screening, and assist with subject arrivals
  • Conduct phlebotomy, specimen processing using universal precautions, and other procedures as appropriate
  • Participate in process improvement activities and develop corrective and preventive action plans
Qualifications Clinical Research Coordinator I
  • Minimum of one year full‑time related experience required
  • Must maintain subject and document confidentiality at all times
  • Understand and comply with sponsor requirements, FDA regulations, Good Clinical Practices (GCP), International Conference on Harmonization (ICH), HIPAA, IRB, and institutional policies and procedures
  • Requires good medical knowledge, including medical terminology and basic subject care
  • May require phlebotomy and vital sign collection skills, as well as the ability to operate centrifuges and EKG machines
  • Preferred:
    Higher education or vocational training specializing in healthcare
  • May require healthcare licensure or other specialized training
Clinical Research Coordinator II
  • Minimum of two years full‑time related experience in clinical research required
  • Must maintain subject and document confidentiality at all times and comply with sponsor requirements, FDA regulations, Good Clinical Practices (GCP), International Conference on Harmonization (ICH), HIPAA, Institutional Review Boards (IRB), and institutional policies and procedures
  • Ability to provide guidance or informal supervision to a Research Assistant or CRC I in the conduct of their study, as applicable
  • Bachelor’s degree and SOCRA or ACRP certification strongly preferred
  • A Master’s degree in clinical research or a related field, or an M.D., may substitute for the two years of clinical research experience
Compensation
  • Clinical Research Coordinator I - $24.67 to $35.78 hourly
  • Clinical Research Coordinator II - $28.85 to $42.98 hourly
Benefits
  • Medical, dental, vision insurance
  • Flexible spending accounts: health care, dependent care, commuter
  • Short and long‑term disability
  • 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 ORCA pass
  • Wellness benefits
  • Voluntary benefits
About Us

The Clinical Research Program at Benaroya Research Institute (BRI) works together with clinicians at Virginia Mason Medical Center to bring clinical research opportunities to patients, giving them access to clinical trials for over 100 different conditions including cancer, digestive…

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