Associate Director, Senior International Clinical Trial Regulatory Lead

Takedajobs

Zurich, Switzerland
Fully remote
8 years of experience in regulatory affairs
Expertise in clinical trial applications
Strong understanding of eu regulatory standards
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 oversee the creation, submission, and maintenance of clinical trial applications globally.
  • The position requires excellent communication skills and the ability to mentor team members.

Matching Summary

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

Skills & Requirements

Must-have

  • 8 years of experience in regulatory affairs
  • expertise in clinical trial applications
  • strong understanding of EU regulatory standards

Nice-to-have

  • experience with non-EU regulatory landscapes
  • ability to manage with limited supervision
  • proficient in GxP audits

Key Requirements

  • BSc or advanced scientific degree preferred
  • experience leading a team
  • in-depth knowledge of Clinical Trials Regulation

Work Rights

Not specified

Tailored Resume

Cover Letter