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Clinical Research Regulatory Coordinator 1

Inova Health System
parental leave, paid time off
United States, Virginia, Fairfax
Feb 15, 2026

Inova Research Center - Cancer team is seeking a dedicated Clinical Research Regulatory Coordinator 1 to join the team. This role will be full-time hybrid day shift from Monday - Friday, Day shift.

Inova is consistently ranked a national healthcare leader in safety, quality and patient experience. We are also proud to be consistently recognized as a top employer in both the D.C. metro area and the nation.

Featured Benefits:

  • Committed to Team Member Health: offering medical, dental and vision coverage, and a robust team member wellness program.

  • Retirement: Inova matches the first 5% of eligible contributions - starting on your first day.

  • Tuition and Student Loan Assistance: offering up to $5,250 per year in education assistance and up to $10,000 for student loans.

  • Mental Health Support: offering all Inova team members, their spouses/partners, and their children 25 mental health coaching or therapy sessions, per person, per year, at no cost.

  • Work/Life Balance: offering paid time off, paid parental leave, flexible work schedules, and remote and hybrid career opportunities.

Clinical Research Regulatory Coordinator 1 Job Responsibilities:

  • Explains the investigational products development process and identify key regulations to control these processes.

  • Explains basic elements of subject safety including the reasoning behind the required use of an Institutional Review Board Independent Ethics Committee, study activity documentation, and event reporting requirements.

  • Performs study regulatory activities in compliance with Good Clinical Practice (GCP), federal regulations, and Inova policies.

  • Coordinates the preparation and submission of new studies to appropriate committees, including the Office of Research at Inova, DSMC, PRMC, IRBs, and other committees as necessary, including drafting and/or editing of informed consent documents.

  • Submits regulatory documents to support initial reviews of studies, continuing reviews, and amendments.

Minimum Requirements:

  • Education: Bachelor's degree preferred. Associates degree required.

  • Experience: One (1) year clinical research experience or Two (2) years clinical experience with Associate degree.

Preferred Requirements:

  • Experience working with research grants.

  • Research and regulatory experience

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