GVP Auditor

Travel: Occasional client site visits (rare)

Contract: Consulting

About the Role

We are looking for an experienced GVP Auditor to join our growing consultancy team. You will provide independent, risk-based assurance that our clients’ pharmacovigilance (PV) systems meet regulatory requirements and protect patient safety.

You’ll work across a wide range of organisations—from start-up biotechs to global pharmaceutical companies—supporting compliance with EU Good Pharmacovigilance Practice (GVP) and expectations from regulators such as the European Medicines Agency .

What You’ll Do

• Plan and deliver risk-based PV audits (system, process, vendor, and affiliate)
• Assess key PV activities, including:
• ICSR processing
• Signal detection and management
• Literature monitoring
• Quality Management Systems
• Oversight of outsourced providers