Regulatory Submissions Manager (eu Ctr)- Turkiye

ICON Clinical Research, LP

Not specified
Lead regulatory activities independently
Experience with cta/ind/maa submissions
Strong understanding of global regulatory requirements
ICON Clinical Research is seeking a Regulatory Submissions Manager with expertise in regulatory affairs, particularly in EU CTR and UK-specific submissions. The role involves leading regulatory activities, providing operational support, and contributing to drug development processes

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization.
  • As a Manager, Regulatory Affairs, you will play a pivotal role in contributing to drug development.
  • ICON offers a range of benefits designed to support well-being and work-life balance.

Matching Summary

Match Score: 85

ICON Clinical Research is seeking a Regulatory Submissions Manager with expertise in regulatory affairs, particularly in EU CTR and UK-specific submissions. The role involves leading regulatory activities, providing operational support, and contributing to drug development processes.

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 scientific field
  • Minimum of 6 years in regulatory affairs
  • Prior experience with regulatory submissions

Work Rights

Not specified

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