Vice President, Regulatory Affairs, Europe And International

BeiGene

Basel, Switzerland
Regulatory strategy development
Market access
Drug development process
The Vice President, Europe and International Regulatory Affairs is responsible for building and leading regulatory groups to develop and implement regulatory strategies for market access

Job Summary

  • The Vice President, Europe and International Regulatory Affairs is responsible for building and leading regulatory groups to develop and implement regulatory strategies for market access.
  • This leadership position involves providing strategic regulatory oversight, interfacing with regulatory bodies like the EMA, and managing a diverse team across a broad geographic area.
  • The role requires extensive knowledge of drug development and regulatory requirements, with a focus on oncology, and involves contributing to high-quality submissions and lifecycle management.

Matching Summary

The Vice President, Europe and International Regulatory Affairs is responsible for building and leading regulatory groups to develop and implement regulatory strategies for market access.

Skills & Requirements

Must-have

  • Regulatory strategy development
  • Market access
  • Drug development process
  • Interaction with Health Authorities
  • Line management responsibility

Nice-to-have

  • Collaborative and passionate interest
  • Leveraging new technologies
  • Supportive team environment
  • Entrepreneurial mindset

Key Requirements

  • Extensive regulatory experience
  • Proven track record of regulatory accomplishments
  • Strong leadership of people
  • Thorough understanding of drug development process

Work Rights

Not specified

Tailored Resume

Cover Letter