Associate Director, Precision Medicine Digital Health

Bristol Myers Squibb UK

Warsaw - pl: zł361,740 - zł438,337 py
Hybrid (50% onsite)
Global regulatory strategy
Biomarker and companion diagnostic development
Digital health solutions regulatory
Bristol Myers Squibb is seeking an Associate Director for Precision Medicine Digital Health, a role focused on leading global regulatory strategies for biomarkers, companion diagnostics, and digital health solutions. The position requires extensive experience in regulatory affairs within the medical device and pharmaceutical sectors, along with strong leadership and project management skills

Job Summary

  • The Associate Director, GRS PMDH leads global regulatory strategies to support the development and approval of biomarkers, companion diagnostic tests, digital health solutions, and other devices associated with pharmaceutical products across therapeutic areas.
  • This role involves assessing regulatory landscapes, managing regulatory risks, and developing global filing strategies.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment and offers a wide variety of competitive benefits, services and programs.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking an Associate Director for Precision Medicine Digital Health, a role focused on leading global regulatory strategies for biomarkers, companion diagnostics, and digital health solutions. The position requires extensive experience in regulatory affairs within the medical device and pharmaceutical sectors, along with strong leadership and project management skills.

Salary

Warsaw - PL: zł361,740 - zł438,337

Skills & Requirements

Must-have

  • Global regulatory strategy
  • Biomarker and companion diagnostic development
  • Digital health solutions regulatory
  • Marketing application submission teams
  • Health Authority query response
  • Clinical trial application response

Nice-to-have

  • Team leadership techniques
  • Cross-functional collaboration
  • Issue resolution and conflict management
  • Quality decision-making
  • Negotiation and influence skills

Key Requirements

  • 7+ years US or EU Medical Device Regulatory Affairs experience
  • Bachelor's degree required
  • Advanced scientific degree preferred

Work Rights

Not specified

Tailored Resume

Cover Letter