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Clinical Trials Data Coordinator
Job Summary
A company is looking for a Clinical Trials Data Coordinator.
Key Responsibilities
- Ensure data integrity for various research studies, including data abstraction and CRF completion
- Coordinate sponsor monitor visits and maintain audit-ready data
- Oversee electronic research records and patient information in the CTMS
Required Qualifications
- Bachelor's Degree, with relevant experience as a substitute
- At least two years of experience in oncology clinical trials
- Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements
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COMPLETE JOB DESCRIPTION
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