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About this Candidate
DAVRON Report for this Director of Clinical Operations:
- Master of Science in Clinical Research Administration with a background in oncology, rheumatology, and radiopharmaceutical trials
- Extensive experience managing clinical trials, overseeing CRAs, CTMs, and cross-functional study teams to ensure GCP compliance and timely execution
- Skilled in investigational product (IP) management, NDA preparation, regulatory submission support, and deviation mitigation
- Proficient in site management, budget planning, and collaboration with CROs, vendors, and regulatory bodies; well-versed in electronic data capture and central lab systems
- Bilingual (English/Spanish) with proven leadership in CRA training, protocol compliance, and operational process improvement initiatives
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