- Uxbridge, England, United Kingdom
- Hybrid
- Manager
- 5+ years
Lead planning and execution of clinical trials across multiple studies, providing scientific and clinical leadership within a global drug development team.
Responsibilities
- Lead planning and execution of all study activities across multiple trials
- Maintain deep protocol expertise and act as the clinical knowledge hub for your study team
- Collaborate on protocol and Informed Consent Form development
- Oversee data generation and validation activities, including CRF design, clinical data review, and query resolution
- Identify clinical data trends and elevate observations to the Medical Monitor
Requirements
- Bachelor's in Life Sciences
- MD
- PhD
- PharmD
- MS