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Global Regulatory Intelligence Manager, slough
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Client:
Warman O'Brien
Location:
slough, United Kingdom
Job Category:
Other
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EU work permit required:
Yes
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Job Views:
3
Posted:
28.06.2025
Expiry Date:
12.08.2025
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Job Description:
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.
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