- Uxbridge, England, United Kingdom
- Hybrid
- Full-time · Manager
- 5+ years
Lead the planning and execution of all study activities across multiple trials, with a high degree of autonomy, providing scientific and clinical leadership to supporting Clinical Scientists.
Responsibilities
- Lead the 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 (ICF) development
- Oversee data generation and validation activities, including CRF design, clinical data review, and query resolution
- Identify clinical data trends and escalate observations appropriately to the Medical Monitor
Requirements
- Degree in Life Sciences
- Nice to have: MD
- Nice to have: PhD
- Nice to have: PharmD
- Nice to have: MS