Corporate Vigilant Associate -cdi- H/f

Pierre Fabre

Boulogne-Billancourt, France
Medical review of vigilance cases
Literature review for risk assessment
Quality control of vigilance data
You will ensure the proper management of pharmacovigilance cases for products under your responsibility on an international scale, from reception to transmission to health authorities, partners, and subsidiaries, while respecting regulatory, contractual, and internal deadlines

Job Summary

  • You will ensure the proper management of pharmacovigilance cases for products under your responsibility on an international scale, from reception to transmission to health authorities, partners, and subsidiaries, while respecting regulatory, contractual, and internal deadlines.
  • You will be responsible for the medical review of vigilance cases from all sources, providing complete and relevant data for signal detection and risk management, managing this process in collaboration with service providers, partners, and clinical study teams.
  • Pierre Fabre offers an attractive compensation and benefits package including profit-sharing, employee stock ownership with matching, health and welfare coverage, RTT days, and public transport assistance.

Matching Summary

You will ensure the proper management of pharmacovigilance cases for products under your responsibility on an international scale, from reception to transmission to health authorities, partners, and subsidiaries, while respecting regulatory, contractual, and internal deadlines.

Skills & Requirements

Must-have

  • Medical review of vigilance cases
  • Literature review for risk assessment
  • Quality control of vigilance data
  • Support for subsidiaries and service providers
  • Digital media vigilance implementation

Nice-to-have

  • Commitment to corporate social responsibility
  • Recognition as a top global employer
  • Employee stock ownership plan participation

Key Requirements

  • 5+ years of experience in pharmacovigilance
  • Higher education in Pharmacy
  • Experience in clinical trial management
  • Fluent English (written and spoken)

Work Rights

Not specified

Tailored Resume

Cover Letter