Pharmacovigilance Specialist
IQVIA · Athens, Greece
SafetyFull-timeCompany career page
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Role summary
IQVIA seeks a Pharmacovigilance Specialist for its Athens office to manage adverse event processing, ensure regulatory compliance, and deliver training. The hybrid, full-time role interfaces with pharmaceutical clients and internal teams while maintaining pharmacovigilance operations and quality standards.
What they're looking for
- Bachelor's degree in Life Sciences, Pharmacy, or related field
- 2+ years of Pharmacovigilance or Drug Safety experience with GVP guideline knowledge
- Fluent in English and Greek
- Strong attention to detail and compliance focus
- Demonstrated training delivery and coordination abilities
- Master's degree or Pharmacovigilance certification (preferred)
What you'll be doing
- Collect, assess, and process Adverse Events, Serious Adverse Events, and Product Quality Complaints
- Perform case intake, triage, data entry, and follow-up with accurate reporting to clients
- Conduct Source Data Verification, reconciliations, and quality checks
- Deliver Pharmacovigilance training programs and onboarding for new team members
- Ensure compliance with EU GVP guidelines, local regulations, and internal standard operating procedures
Privacy & handoff
This role links to IQVIA'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.