Regulatory Affairs Manager

IQVIA Inc

France
3+ years regulatory affairs experience
French pharmaceutical legislation knowledge
Native french and fluent english skills
This role involves managing country-level regulatory activities for medicinal products to ensure full compliance with local requirements in France

Job Summary

  • This role involves managing country-level regulatory activities for medicinal products to ensure full compliance with local requirements in France.
  • The successful candidate will prepare and coordinate regulatory submissions including notifications, renewals, variations, and new applications.
  • IQVIA offers a global team environment dedicated to driving smarter healthcare and supporting continuous career growth through learning.

Matching Summary

This role involves managing country-level regulatory activities for medicinal products to ensure full compliance with local requirements in France.

Skills & Requirements

Must-have

  • 3+ years regulatory affairs experience
  • French pharmaceutical legislation knowledge
  • Native French and fluent English skills

Nice-to-have

  • Experience with centralized activities
  • Strong organizational and detail skills
  • Collaborative working style

Key Requirements

  • Bachelor of Pharmacy or Life Sciences degree
  • 3+ years experience on French market
  • Excellent knowledge of French pharmaceutical legislation

Work Rights

Not specified

Tailored Resume

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