- Remote, United Kingdom
- Remote
- Full-time
- 10+ years
Provide medical and scientific oversight for clinical trials, serve as Medical Monitor, support protocol development, safety monitoring, data review, and business development activities for oncology/hematology studies.
Responsibilities
- Provide medical and scientific input to clinical research programs
- Ensure medical activities comply with GCP
- Develop and review study protocols and safety plans
- Provide on‑call coverage for protocol queries
- Review and analyze safety data and adverse events
Requirements
- Medical Degree from an accredited medical school
- Nice to have: 3-5 years biopharmaceutical industry experience
- Nice to have: Oncology/Hematology specialization
- Nice to have: Board Certified/Eligible in Oncology