Vigilant Expert(e) -cdi- H/f

Naturactive

Boulogne, France
**
5 years experience in pharmacovigilance
Expertise in clinical trial safety
Strong knowledge of regulatory compliance
** Pierre Fabre is seeking a Vigilant Expert to join its pharmacovigilance team in Boulogne or Toulouse, with a focus on ensuring patient safety and compliance for products in development and those already on the market. The ideal candidate should have a medical or pharmaceutical background, a minimum of five years of experience in pharmacovigilance, and familiarity with clinical trial safety assessments. **

Job Summary

  • You will be responsible for pharmacovigilance of products under development and in clinical trials.
  • The role involves risk management and communication of safety information to authorities.
  • This position offers attractive compensation and benefits, including telework options.

Matching Summary

Match Score: 75

** Pierre Fabre is seeking a Vigilant Expert to join its pharmacovigilance team in Boulogne or Toulouse, with a focus on ensuring patient safety and compliance for products in development and those already on the market. The ideal candidate should have a medical or pharmaceutical background, a minimum of five years of experience in pharmacovigilance, and familiarity with clinical trial safety assessments. **

Skills & Requirements

Must-have

  • 5 years experience in pharmacovigilance
  • Expertise in clinical trial safety
  • Strong knowledge of regulatory compliance

Nice-to-have

  • Experience in oncology or orphan drugs
  • Ability to work in an international environment
  • Proficiency in digital tools and databases

Key Requirements

  • Medical or Pharmacy degree
  • Fluent in English
  • Experience with safety signal detection

Work Rights

Not specified

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