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