PV Specialist (m/f/d) - Greece
HybridCholargós, Attica, Greece
Job Summary
Collect, assess, document, process, and report adverse events and safety information in compliance with regulations and company procedures. Ensure timely handling and follow-up of safety reports, perform reconciliations to identify and escalate discrepancies, and maintain accurate, audit-ready documentation. Support pharmacovigilance activities for Patient Support Programs, review program documentation and contracts, deliver training for internal and external teams, and contribute to audits, CAPAs, and continuous process improvement. Collaborate with cross-functional teams and stakeholders to support patient safety activities. This role requires a University Degree in Life Sciences or related field with at least one year of PV experience, solid GVP knowledge, and fluency in English and the local language.
Required Qualifications
- University Degree in Life Sciences, Pharmacy, Nursing, Medicine, or a related field
- At least 1+ years of experience in Pharmacovigilance, Drug Safety, or a related role within a Pharmaceutical or CRO company
- Solid working knowledge of Good Pharmacovigilance Practices (GVP), ICH guidelines, and global/local adverse event reporting requirements (e.g., EMA, FDA, national competent authorities)
- Hands-on experience with safety databases
- Very good verbal and written communication skills, with the ability to prepare clear, accurate, and audience-appropriate safety documentation
- Fluent in the local language and English, both written and verbal
- Strong attention to detail and ability to independently manage sensitive and complex data
- Excellent organizational and time-management abilities
- Advanced computer literacy
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