Supervisor, Pharmacovigilance (Safety reporting)
ICON · Sofia, Bulgaria +1 more
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Role summary
This role supervises pharmacovigilance safety reporting operations for clinical trials and marketed products, ensuring regulatory compliance and timely adverse event reporting. The supervisor will lead a team, coordinate with cross-functional departments, and manage safety submissions to regulatory authorities. Candidates need 8+ years in drug safety or pharmacovigilance, a life science degree, and proven team management capabilities.
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.