$226,750 – $313,460
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 senior regulatory leadership role at a major pharmaceutical company guiding the development and commercialization of neuroscience drugs globally. This position suits experienced regulatory professionals with scientific backgrounds who can navigate complex drug development, interface with health authorities, and lead strategic initiatives across multiple markets.
Our summary, not Bristol Myers Squibb’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- Advanced degree in scientific discipline (MD, PhD, or PharmD preferred)
- 8-12 years pharmaceutical industry experience
- 6-8 years regulatory affairs experience
- Thorough knowledge of drug research, development, and commercialization
- US regulatory expertise and EU background desired
- Global experience preferred
- Inter-dependent partnering and team-oriented approach
- Cross-cultural competency
- Strong organizational, communication, and time management skills
- Ability to manage multiple projects simultaneously
- Capacity to innovate and solve complex business problems
Nice to have
- Experience in neurology, neuromuscular diseases, or neuropsychiatry drug development
- Demonstrated expertise in drug development, CMC, pharmacotoxicology, biopharmaceutics, clinical, or promotional areas