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:

• Extensive experience in regulatory affairs within Clinical Trials and/or unlicensed supply.
• Strong knowledge of global regulatory frameworks and legislation.
• Ability to analyse and communicate complex regulatory data effectively.
• Proficiency in Microsoft Office and regulatory tools/databases.
• Highly organised, detail-oriented, and proactive with excellent communication skills.
• Science or health-related degree preferred.

This is an excellent opportunity for a regulatory professional who is motivated by meaningful work that directly impacts patient lives. The organisation fosters a collaborative and supportive culture, where initiative and expertise are valued.