Pharmacovigilance Associate

ICON seeks a Pharmacovigilance Associate to monitor pharmaceutical product safety by collecting, analyzing, and reporting adverse events. The role involves processing safety data, managing queries, and collaborating with cross-functional teams to ensure compliance with regulatory standards.

Responsibilities

• Collect, process, and enter serious adverse events into safety database
• Conduct quality control and write narratives for case finalization
• Raise and manage queries for missing information and discrepancies
• Reconcile safety events between safety and clinical databases
• Prepare study documents and support safety-related investigations

Requirements

• Bachelor's degree in relevant scientific or healthcare discipline
• Pharmacovigilance or drug safety experience in clinical or pharmaceutical environment
• Ability to review and process safety events
• Experience with safety database systems
• Strong analytical skills with attention to detail
• Fluent English with excellent communication and interpersonal abilities
• Commitment to quality and compliance standards