California Licensed Clinical Trials Coordinator
Job Summary
Ensuring data integrity for various research studies, the full-time remote California Licensed Clinical Trials Coordinator will manage data abstraction, CRF completion, query resolution, and sponsor monitor visit coordination while overseeing electronic research records and patient information in the CTMS.
Key responsibilities
- Ensure data integrity by performing data abstraction and completing CRFs
- Coordinate sponsor monitor visits and resolve queries related to study data
- Maintain audit-ready data and oversee electronic research records in the CTMS
Required qualifications
- Bachelor's Degree, with relevant experience considered as a substitute
- At least two years of experience related to the conduct of oncology clinical trials
- Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements
- In-depth knowledge of Good Clinical Practices (GCP) and FDA regulations
- Ability to communicate protocol deviations or issues effectively
Complete Job Description
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