# Associate Director, Global Scientific and Regulatory Documentation, Content Strategy

Hiring organization: [Bristol Myers Squibb](https://career.thegoodapps.co/organizations/bristol-myers-squibb)

Canonical page: https://career.thegoodapps.co/jobs/fe02c300-e1e4-45e2-8f30-6388c6d7b831

Listed on Bristol Myers Squibb's own careers site. Applications go to them directly.

- Employment type: full time
- Seniority: Senior
- Location: Princeton, NJ
- Salary: 170880 – 207061 USD per year

## Summary

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._

## Skills named

Drug Development

## 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

Apply on Bristol Myers Squibb's site: https://bristolmyerssquibb.wd5.myworkdayjobs.com/en-US/BMS/job/Princeton---NJ---US/EG-140---Regulatory-Affairs---Medical-Writing_R1604781