Clinical Research Coordinator: Study Ops & Patient Impact
Listed on 2026-10-07
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Healthcare
Clinical Research -
Research/Development
Clinical Research
The Clinical Trials Center of Middle Tennessee, LLC seeks a motivated Clinical Research Coordinator (CRC) to support the Principal Investigator in daily trial activities, ensure protocol compliance, and coordinate data collection, scheduling, and regulatory documentation.
You will work with the research team, sponsor, and participants, managing source documents, adverse events, and study timelines while maintaining patient safety and IRB requirements.
Consider building your career as a Clinical Research Coordinator:
Study Ops & Patient Impact at CLINICAL TRIALS CENTER OF MIDDLE T.
As a Clinical Research Coordinator:
Study Ops & Patient Impact, you will play an important part at CLINICAL TRIALS CENTER OF MIDDLE T in Franklin, TN, United States.
We invite applications for the Clinical Research Coordinator:
Study Ops & Patient Impact position located in Franklin, TN, United States.
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