$215,130 – $291,964
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
A leadership role overseeing global and US regulatory strategy for drug development programs, working across internal teams and external partners to navigate approvals and bring products to market. This suits experienced regulatory professionals ready to own complex, multi-market registration strategies and lead cross-functional teams at scale.
Our summary, not Bristol Myers Squibb’s wording. The full posting is on their site.
What they ask for
Required
- Ph.D., M.D., PharmD, MS, or BS in a scientific discipline
- 4-7+ years of regulatory affairs experience
- Proven track record delivering global regulatory strategies leading to product registration
- Ability to communicate regulatory strategy and risk in written and verbal formats
- Experience leading cross-functional matrix teams
- Ability to translate complex scientific issues into regulatory implications
- Experience negotiating with health authorities
Nice to have
- Experience with simultaneous global filings