- Location
- Chiswick, London, UK · Remote, UK
- Workplace
- Hybrid, Remote
- Type
- Full-time
- Department
- Regulatory Affairs
- Seniority
- Entry
- Source
- Lever
Description
Are you seeking an exciting and fulfilling new opportunity? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring forward ideas that make a real difference. Be part of a mission-driven organisation dedicated to advancing clinical research and transforming lives.
Role Objectives:
The WEP Clinical Associate Director of Regulatory Affairs is responsible for understanding,
developing, and leading the Regulatory Affairs strategy for Global Expanded Access Programs
(EAP), Open Label Extension (OLE), and Post-Approval Named Patient Programs (PA-NPP).
developing, and leading the Regulatory Affairs strategy for Global Expanded Access Programs
(EAP), Open Label Extension (OLE), and Post-Approval Named Patient Programs (PA-NPP).
