Manager, International Clinical Trial Regulatory Lead

Takedajobs

Zurich, Switzerland
Regulatory affairs experience
Knowledge of cta regulations
Collaboration with cros
The role involves contributing to the regulatory strategy for clinical trials in Europe and Canada

Job Summary

  • The role involves contributing to the regulatory strategy for clinical trials in Europe and Canada.
  • You will oversee the creation and submission of clinical trial applications in compliance with legal requirements.
  • Collaboration with global and regional counterparts is essential to manage all aspects of assigned regulatory activities.

Matching Summary

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

Skills & Requirements

Must-have

  • regulatory affairs experience
  • knowledge of CTA regulations
  • collaboration with CROs

Nice-to-have

  • ability to adapt to changing circumstances
  • promotes an inclusive culture
  • strong analytical skills

Key Requirements

  • minimum of 3 years experience
  • BSc or advanced scientific degree preferred
  • fluency in English

Work Rights

Not specified

Tailored Resume

Cover Letter