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.
What You Will Be Doing
- Supervising the day-to-day pharmacovigilance operations, ensuring timely and accurate reporting of adverse events.
- Collaborating with cross‑functional teams, including clinical operations and regulatory affairs, to optimize pharmacovigilance processes.
- Ensuring compliance with global regulatory requirements and internal standard operating procedures for safety reporting.
- Managing safety data collection, analysis, and submission to regulatory authorities.
- Providing leadership and training to the pharmacovigilance team, ensuring adherence to best practices in safety monitoring.
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