Associate Director, Senior International Clinical Trial Regulatory Lead

Takeda

Zurich, Switzerland
Fully remote
Regulatory strategy development
Clinical trial applications management
Experience in regulatory affairs
The role involves contributing to regulatory strategy for clinical trials in Europe and Canada

Job Summary

  • The role involves contributing to regulatory strategy for clinical trials in Europe and Canada.
  • You will manage all aspects of clinical trial applications throughout the development lifecycle.
  • The position requires collaboration with CROs to ensure compliance with regulatory requirements.

Matching Summary

The role involves contributing to regulatory strategy for clinical trials in Europe and Canada.

Skills & Requirements

Must-have

  • Regulatory strategy development
  • Clinical trial applications management
  • Experience in regulatory affairs

Nice-to-have

  • Strong leadership skills
  • Ability to mentor team members
  • Proactive communication skills

Key Requirements

  • Minimum 8 years of regulatory experience
  • Advanced scientific degree preferred
  • Experience with Clinical Trials Regulation

Work Rights

Not specified

Tailored Resume

Cover Letter