What are the responsibilities and job description for the Director of Medical Evidence Generation position at Bristol-Myers Squibb?
We are seeking a highly skilled Director of Medical Evidence Generation to join our team at Bristol Myers Squibb. As a Director of Medical Evidence Generation, you will play a critical role in leading the development and execution of strategies to generate high-quality medical evidence to support the development and approval of our innovative medicines.
The ideal candidate will have a strong background in clinical research, medical writing, or a related field, and excellent communication and interpersonal skills. They will work closely with cross-functional teams, including medical affairs, development, commercial, regulatory affairs, legal, and compliance, to ensure seamless program execution and compliance with global, regional, and local regulations and guidelines.
Key Responsibilities:
- Lead the development and execution of strategies to generate high-quality medical evidence to support the development and approval of our innovative medicines
- Collaborate with key partners to define and develop the medical evidence strategy for assets across multiple diseases
- Ensure the medical evidence strategy has input from all required partners and goes through the appropriate review and governance processes
- Partner with GDO/RCO to ensure seamless operationalization of medical evidence programs for their respective disease areas, ensuring appropriate country rules are followed
- Implement standardized policies, procedures, and best practices across the portfolio of medical evidence programs
