Pharmacovigilance Specialist

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