Pharmacovigilance Supervisor
About this role
About the Role ICON is seeking a Pharmacovigilance Supervisor to oversee safety monitoring and reporting of adverse events for clinical trials and marketed products. You will lead pharmacovigilance operations, ensure regulatory compliance, and collaborate with cross-functional teams to maintain high standards of patient safety. What You'll Do
- 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.
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