Pharmacovigilance Specialist
View: 104
Update day: 07-12-2025
Location: Waterloo Walloon Brabant
Industry: Pharmaceutical Manufacturing Biotechnology Research
Position: Mid-Senior level
Job type: Full-time
Job content
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
Deadline: 21-01-2026
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