Pharmacovigilance Auditor - Freelance Position (1FTE or 0.6 FTE and above)
Full-time
Department: GVP Compliance
Medicine moves forward here. ADAMAS Consulting helps the world's pharmaceutical and biotechnology companies uphold the highest standards of quality, compliance and patient safety. We think of our work as more than auditing. ADAMAS Consulting is looking for PV Auditor on a freelance basis to cover audits across Europe. Both full and part time (0.6+ FTE) will be considered
Planning, preparation, conduct, reporting and follow up (including CAPA plans) of various types of Pharmacovigilance (PV) audits according to expected quality and timelines
Executing audits based on a comprehensive understanding of all regulatory requirements and Good Pharmacovigilance Practice (GVP)




Performing GVP quality assurance projects on behalf of client companies within the pharmaceutical/biotechnology industry.
Experience in conducting and leading internal and external Pharmacovigilance audits for a variety of stakeholders
Expert knowledge of national and international Pharmacovigilance legislation and guidelines
Proficient in managing projects and ensuring deliverables are provided timeously
Bachelor's Degree in Life Sciences preferred
Travel will be required for audits, additional to conducting remote audits
You'll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.
Quality: we hold ourselves to the standard patients deserve.

📌 Pharmacovigilance Auditor (Madrid)
🏢 Adamas Consulting
📍 Madrid