# Associate Director, GRS Heme/Onc

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

Canonical page: https://career.thegoodapps.co/jobs/32039726-32ea-4f92-84af-fa76abccf70a

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

- Employment type: full time
- Seniority: Senior
- Location: Princeton, NJ
- Salary: 173350 – 210058 USD per year

## Summary

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._

## 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

Apply on Bristol Myers Squibb's site: https://bristolmyerssquibb.wd5.myworkdayjobs.com/en-US/BMS/job/Princeton---NJ---US/Associate-Director--GRS-Heme-Onc_R1603320