Associate Director, Global Scientific and Regulatory Documentation, Content Strategy
Bristol Myers SquibbPrinceton, NJ · full time · Senior
$170,880 – $207,061
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 involves authoring and coordinating complex regulatory documents for clinical drug submissions across immunology and cardiovascular programs, ensuring compliance with global regulatory standards and internal documentation practices. The position suits experienced pharmaceutical professionals with strong scientific writing skills who can lead cross-functional teams and manage documentation strategy from early development through marketing authorization.
Our summary, not Bristol Myers Squibb’s wording. The full posting is on their site.
What they ask for
Required
- PharmD, PhD, MD in relevant scientific discipline OR Master's/Bachelor's degree with ~10 years pharmaceutical regulatory documentation experience
- Expert writing skills in clinical and regulatory documents including registrational submissions
- Ability to analyze and interpret complex scientific data across disciplines
- Thorough understanding of global pharmaceutical drug development and major regulatory submission requirements
- Strong organizational, communication, facilitation and interpersonal skills in cross-functional teams
- Working knowledge of document management systems and basic publishing process knowledge
Nice to have
- Experience with state-of-the-art documentation processes and technology