Travel- Clinical Research Regulatory Coordinator
Listed on 2026-09-30
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Healthcare
Clinical Research
Central Ohio Urology Group seeks a Clinical Research Regulatory Coordinator to maintain regulatory documents and ensure ICH-GCP adherence across sites. You will support staff documentation, certifications, and site readiness for inspections, while coordinating IRB submissions and continuing reviews.
The role requires 2–5 years of clinical research experience, strong communication, superb organizational skills, and willingness to travel to multiple sites.
We have an opening for a Travel-Ready Clinical Research Regulatory Coordinator in TN, United States within Legal, Management & Operations.
All applications are reviewed carefully by our team.
The position is based in TN, United States.
This opportunity is part of our work in Legal, Management & Operations.
The advertised compensation is 65.000 - 85.000.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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