$173,350 – $241,566
Listed on Bristol Myers Squibb’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role leads the development and execution of global regulatory strategies for oncology drugs through their full lifecycle, managing FDA submissions and coordinating with cross-functional teams. It suits experienced regulatory affairs professionals with a scientific background who can navigate complex drug development processes and influence outcomes across organizational boundaries.
Our summary, not Bristol Myers Squibb’s wording. The full posting is on their site.
What they ask for
Required
- PhD, MD, Pharm.D., BS or MS degree in a scientific field
- 4-8 years pharmaceutical industry experience
- 3-5 years regulatory affairs experience
- Knowledge of drug development, IND and NDA processes
- Experience preparing FDA submissions
- Strong experience with US regulatory submissions and dossiers
- Team leadership experience
- Problem-solving and analytical skills
- Attention to detail
Nice to have
- Travel availability