# Associate Director Global Regulatory Sciences - Oncology

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

Canonical page: https://career.thegoodapps.co/jobs/87c5fd51-cf75-456f-acf0-922d1c40d5ba

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

- Employment type: full time
- Seniority: Director
- Salary: 173350 – 241566 USD per year

## Summary

This role leads the development and execution of global regulatory strategies for oncology drugs through their full lifecycle, managing FDA submissions and coordinating with cross-functional teams. It suits experienced regulatory affairs professionals with a scientific background who can navigate complex drug development processes and influence outcomes across organizational boundaries.

_Our summary, not Bristol Myers Squibb's wording._

## Skills named

Project Management

## Required

- PhD, MD, Pharm.D., BS or MS degree in a scientific field
- 4-8 years pharmaceutical industry experience
- 3-5 years regulatory affairs experience
- Knowledge of drug development, IND and NDA processes
- Experience preparing FDA submissions
- Strong experience with US regulatory submissions and dossiers
- Team leadership experience
- Problem-solving and analytical skills
- Attention to detail

## Nice to have

- Travel availability

Apply on Bristol Myers Squibb's site: https://bristolmyerssquibb.wd5.myworkdayjobs.com/en-US/BMS/job/Princeton---NJ---US/Associate-Director-Global-Regulatory-Sciences---Oncology_R1603517