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Senior Research Coordinator
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Full-time
- 3 years of experience in clinical research with knowledge about the conduct of clinical trials, research principles, and methodologies/study design
- ARUP Handling, Packaging and Shipping Infectious Substances or similar within 30 days of employment if role requires specimen acquisition
- Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA) Certified Research Associate (CRA), Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC) within 1 year of employment
- Coordinates educational activities related to study needs for study staff, investigator team, and patient care staff.
- Ensures Institutional Review Board preparation, submission, modifications, reporting, and termination activities.
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