Associate Director, Eucan Regulatory Lead - Oncology

Takeda

Zurich, Switzerland
Fully remote
Regulatory strategy development
Oncology portfolio management
Experience with health authorities
This role is crucial for Takeda's growing oncology portfolio, focusing on regulatory strategy within the EUCAN region

Job Summary

  • This role is crucial for Takeda's growing oncology portfolio, focusing on regulatory strategy within the EUCAN region.
  • You will support regulatory activities from development to approval, ensuring timely submission and approval of applications.
  • The position involves leading interactions with health authorities and providing strategic guidance to project teams.

Matching Summary

This role is crucial for Takeda's growing oncology portfolio, focusing on regulatory strategy within the EUCAN region.

Skills & Requirements

Must-have

  • Regulatory strategy development
  • Oncology portfolio management
  • Experience with Health Authorities

Nice-to-have

  • Experience with advanced therapeutic products
  • Strong communication skills
  • Ability to manage multiple projects

Key Requirements

  • Minimum 8 years in drug regulatory affairs
  • Advanced scientific degree preferred
  • Experience with cell and gene therapy

Work Rights

Not specified

Tailored Resume

Cover Letter