Senior Pharmacovigilance Associate
ICON · Warsaw, Poland +1 more
SafetyFull-timeCompany career page
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Role summary
Senior Pharmacovigilance Associate role managing drug safety deliverables and adverse event reporting for a global healthcare organization. The position involves overseeing pharmacovigilance activities, analyzing safety data, and ensuring regulatory compliance across multiple markets.
What they're looking for
- Bachelor's degree in scientific or healthcare-related discipline
- Extensive pharmacovigilance or drug safety experience with regulatory knowledge
- Proficiency in pharmacovigilance databases and Microsoft Office Suite
- Strong analytical skills for complex data interpretation and signal detection
- Demonstrated ability to manage adverse event reporting independently
- Excellent cross-functional communication and collaboration abilities
- Willingness to travel approximately 15% as required
What you'll be doing
- Lead collection, evaluation, and processing of adverse event reports per regulatory guidelines
- Analyze safety data to identify trends and potential safety signals requiring investigation
- Prepare and submit periodic safety update reports and regulatory documentation
- Collaborate with medical teams to assess clinical relevance of adverse events
- Maintain pharmacovigilance database integrity and ensure data management compliance
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.