Regulatory Submissions Manager (eu Ctr)- Turkiye

ICON Broadbean

Turkey
Lead regulatory activities independently
Experience with cta/ind/maa submissions
Strong understanding of global regulatory requirements
As a Manager, Regulatory Affairs at ICON, you will play a pivotal role in contributing to drug development

Job Summary

  • As a Manager, Regulatory Affairs at ICON, you will play a pivotal role in contributing to drug development.
  • You'll provide regulatory guidance and operational support across various stages of drug development.
  • ICON is committed to providing a workplace free of discrimination and harassment.

Matching Summary

As a Manager, Regulatory Affairs at ICON, you will play a pivotal role in contributing to drug development.

Skills & Requirements

Must-have

  • Lead regulatory activities independently
  • Experience with CTA/IND/MAA submissions
  • Strong understanding of global regulatory requirements

Nice-to-have

  • Experience with companion diagnostics
  • Ability to develop best practices
  • Collaborative team player

Key Requirements

  • Bachelor's degree in a scientific field
  • Minimum of 6 years of experience in regulatory affairs
  • Prior experience with various regulatory submissions

Work Rights

Not specified

Tailored Resume

Cover Letter