Position: Mid-Senior level

Jobtyp: Full-time

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Jobinhalt

About the Role

We are seeking a detail-oriented and proactive Pharmacovigilance (PV) professional to support day-to-day safety operations within a global pharmaceutical environment. This is a hands-on, operational role focused on ensuring the quality and compliance of outsourced case processing activities. The successful candidate will join a collaborative team and contribute to maintaining high standards in patient safety reporting.

Key Responsibilities

  • Perform quality reviews of Individual Case Safety Reports (ICSRs) processed by external vendors
  • Support literature screening activities and ensure accurate documentation
  • Maintain compliance with global pharmacovigilance regulations and internal SOPs
  • Collaborate with cross-functional teams to ensure timely and accurate safety data handling
  • Assist in audit readiness and regulatory inspections
  • Contribute to continuous improvement initiatives within PV operations

Requirements

  • Bachelor’s degree in Life Sciences or a related field
  • 1–3 years of experience in pharmacovigilance (PV), ideally in a case processing capacity
  • Solid understanding of adverse event reporting and PV regulations
  • Hands-on experience with Argus Safety Database
  • Strong attention to detail and organizational skills
  • Ability to work independently and manage multiple priorities
  • Excellent communication skills in English; French is a cultural asset
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Frist: 21-01-2026

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