Principal Regulatory Strategist (CRO/Pharma Industry) - Europe

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Principal Regulatory Strategist (CRO/Pharma Industry) - Europe, London

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Client:

MMS Holdings Inc.

Location:

London, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

fd1941726a11

Job Views:

4

Posted:

18.07.2025

Expiry Date:

01.09.2025

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Job Description:

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains an industry-leading customer satisfaction rating and fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team shaping the future of clinical research.

Discover more about our opportunities and why MMS is a great place to advance your career. Visit or follow MMS on .

Principal Regulatory StrategistResponsibilities

• Provide consulting and advisory services for complex regulatory issues or projects.
• Author and maintain documentation to ensure regulatory compliance.
• Provide senior technical review for complex regulatory projects.
• Conduct regulatory intelligence gathering to support development of regulatory roadmaps, feasibility assessments, and reports.
• Participate in project teams and provide expertise on regulatory matters.
• Communicate clearly and accurately with peers, supervisors, and stakeholders.
• Implement new or updated operational strategies to comply with policies and recommendations.
• Identify new policies and provide opinions on regulatory changes through blogs, webinars, etc.

Requirements

• College graduate in Biological Science, Public Health, Regulatory Science, or related field; Masters or PhD preferred.
• Minimum of 15 years’ experience in Regulatory Affairs or Strategy, including experience with EMA Marketing Applications.
• Expert knowledge of scientific principles and concepts.
• Reputation as an emerging leader with sustained performance.
• Proficiency in MS Office applications.
• Experience with clinical trials and pharmaceutical development preferred.
• Good communication skills and team-oriented approach.
• Excellent problem-solving skills.
• Strong organizational skills.
• Basic understanding of CROs, clinical data, and drug development process.

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