Job Description
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
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