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Role Objectives:
- Serve as primary medical expert for clinical trial protocols and EAPs.
- Guide investigators and teams on protocol implementation and adherence.
What You'll Do:
- Monitor trials for safety, data accuracy, and protocol compliance.
- Lead protocol development, investigator meetings, and study training.
What You'll Need:
- MD degree with 5+ years of clinical research experience.
- Proven experience in protocol development and safety monitoring.
WEP Clinical
WEP Clinical partners with biopharmaceutical sponsors to deliver clinical trials, expanded access programs, and market access solutions. With 15+ years of experience across 150+ countries, they offer operational scale and a personalised culture.