Offer summary
Qualifications:
4-year degree in Life Science, 8+ years of clinical trial management experience, 1-3 years supervisory experience, Knowledge of FDA regulations and ICH guidelines, Experience in Phase 3 clinical trials preferred.
Key responsabilities:
- Oversee operational aspects of clinical studies
- Manage study budgets, timelines, and vendor relations
- Prepare and review study documents and metrics
- Ensure compliance with protocols and regulations
- Lead cross-functional teams and vendor selection