Pharmacovigilance Associate

Pharmacovigilance Associate (Hands-on experience in Clinical Trial & Post Marketing case processing) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Pharmacovigilance Associate at ICON, you will monitor and ensure the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information.

What You Will Be Doing

• Collect, assess, and process adverse event reports to ensure accuracy and timely compliance with regulatory requirements

• Partner with cross-functional teams to address safety-related questions and support ongoing investigations

• Maintain current knowledge of pharmacovigilance regulations, global safety guidelines, and industry standards

• Manage safety inbox and acknowledge case receipt.

• Perform case triage and book-in to safety database.

• Enter case details accurately and write narratives.

• Code events, drugs, and medical history using MedDRA/WHO-DD.

• Apply correct product labeling and perform QC checks.

• Finalize case processing and generate queries for follow-up