California Licensed Clinical Trials Coordinator
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Job Summary
Ensuring data integrity for various research studies, the full-time remote California Licensed Clinical Trials Coordinator will manage data abstraction, CRF completion, and sponsor monitor visit coordination while maintaining audit-ready data.
Key responsibilities
- Oversee electronic research records and patient information in the CTMS
- Communicate protocol deviations or issues related to study execution
- Maintain adherence to study protocols and ensure proper execution of study parameters
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
Complete Job Description
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