$173,350 – $210,058
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 regulatory strategy and oversees FDA submissions for hematology and oncology drug development at a major pharmaceutical company. It suits experienced regulatory professionals with scientific credentials who can manage complex submissions, lead teams, and coordinate across functions.
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 in regulatory science
- 4-8 years pharmaceutical industry experience
- 3-5 years regulatory affairs experience
- Thorough knowledge of drug development and IND/NDA processes
- Strong US regulatory submissions and dossier experience
- Team leadership experience
- Ability to work with minimal supervision and manage details
- Project management and meeting management skills
Nice to have
- Experience with global submission and Health Authority interaction plans
- Experience applying project management techniques
- Experience coordinating global activities
- Experience with regulatory strategy development tied to clinical and marketing plans