Global Regulatory Intelligence Manager - Clinical Trials/unlicensed supply management
Location: Remote/Hybrid (UK-based)
Job Type: Permanent, Full-time
Regulatory Intelligence Manager with experience in regulatory affairs within Clinical Trials and/or unlicensed supply, required to join a global, compliance-driven environment focused on access to unlicensed and investigational medicines. The successful candidate will play a key role in gathering, maintaining, and interpreting critical regulatory intelligence, supporting global Managed Access and Clinical Trial programmes.
Key Responsibilities:
* Maintain and update regulatory databases and country-specific intelligence.
* Conduct in-depth research on international regulatory pathways (eg EAPs, CUPs, PA-NPPs, Clinical Trials).
* Monitor and interpret regulatory changes across key markets.
* Liaise with vendors and regulatory agencies to obtain accurate, up-to-date intelligence.
* Support strategic planning and compliance through impactful analysis and clear communication of findings.
* Present regulatory insights and risk assessments to internal stakeholders.
* Contribute to improving internal regulatory intelligence processes and tools.
Requirements:
1. Extensive experience in regulatory affairs within Clinical Trials and/or unlic...