Job Details

Global Regulatory Intelligence Manager

5804
  • £Competitive
  • London, Greater London, United Kingdom
  • Permanent

Global Regulatory Intelligence Manager

Location: London (Hybrid)

 

Are you a regulatory affairs professional with a sharp eye for global trends and a passion for making complex information actionable? A dynamic organisation in the healthcare space is seeking a Global Regulatory Intelligence Manager to lead its efforts in gathering, analysing, and applying regulatory insights that impact access to innovative treatments worldwide.

 

About the Role

This is a unique opportunity to shape and support regulatory strategy across unlicensed medicines, clinical trials, and commercial access programs. You’ll act as a central source of intelligence, keeping internal teams well-informed on emerging regulations, potential risks, and new opportunities that affect project execution and patient access.

 

Key Responsibilities

  • Maintain and enhance regulatory intelligence databases, ensuring global accuracy and timeliness.
  • Conduct in-depth research into evolving regulations and provide strategic insights to project teams.
  • Monitor a range of regulatory sources - from agency websites to expert networks - to stay ahead of global trends.
  • Manage relationships with external vendors, ensuring high-quality and cost-effective intelligence support.
  • Translate complex regulatory information into clear, actionable summaries for stakeholders.
  • Collaborate cross-functionally to assess how regulatory shifts may impact key projects.
  • Establish and refine internal intelligence processes that support robust compliance and operational readiness.

 

What We're Looking For

  • Bachelor’s degree in a health or science discipline preferred.
  • Minimum 4 years' experience in regulatory affairs, preferably involving clinical trials or unlicensed medicine supply.
  • Strong ability to interpret legislation and regulatory guidance across diverse markets.
  • Skilled in research, analysis, and communication of regulatory information.
  • Well-organised, detail-oriented, and comfortable working in a fast-paced environment.
  • Adept at working independently and navigating ambiguity with confidence.
  • Strong interpersonal skills with the ability to collaborate and influence across teams.

 

What You’ll Gain

  • A key role in an organisation committed to advancing access to treatment globally.
  • The chance to work at the intersection of compliance, strategy, and global health.
  • A collaborative, forward-thinking environment that values initiative and insight.

 

Interested? Apply now or send your CV to megan@warmanobrien.com.

Megan Stoddart Recruitment Consultant in Medical Affairs

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