Job Description
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 Supervisor, Pharmacovigilance at ICON, you will oversee the safety monitoring and reporting of adverse events related to clinical trials and marketed products.
What You Will Do
You will manage day-to-day pharmacovigilance and drug safety activities, supporting your team to deliver quality outcomes.
Key Responsibilities Include
- 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...