Pharmacovigilance Associate (Clinical Trials)

Pharmacovigilance Associate (Clinical Trials) - Hybrid - Manila

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

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 Do:

Your role will involve delivering pharmacovigilance and drug safety work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

• Collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines.
• Conducting signal detection and risk assessment activities to identify potential safety issues.