Senior Regulatory Affairs Officer
Reading, United Kingdom Regular Posted on May. 21, 2026 Closing on Jun. 16, 2026Job Title: Senior Regulatory Affairs Officer
Location: Reading, UK
Working Pattern: 3 days onsite in Reading, 2 days remote per week
About This Job
As Senior Regulatory Officer - Promotional & Non-Promotional Materials Review within our UK and Ireland Regulatory Affairs Department, you'll lead the delivery of high-quality promotionaland non-promotionalreview services, ensuring all materials comply with relevant legal requirements and Codes of Practice while providing expert support to franchise teams across our diverse portfolio spanning neurological diseases, diabetes, respiratory, cardiovascular, oncology and rare diseases. Ready to get started?
Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.
About Sanofi
We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.
Main Responsibilities
Review promotional and non-promotional materials,in a timely manner,providing constructivecomments and feedbackto ensure they meet legal requirements, industry codes of practice, and company standards
Build strong working relationships with marketing, medical, and governance colleagues to provide timely regulatory advice and support brand planning activities
Mentor/coach team members on regulatory processes, compliance requirements, and best practices
Maintain and update prescribing information, guidance documents, and digital content to ensure accuracy and compliance
Collaborate withkey stakeholdersto find practical solutions to material review challenges while balancing innovation with regulatory requirements
Lead team projects and provide training to internal stakeholders on material review processes and systems
Engage with health authorities when needed for pre-vetting of materials and contribute to the resolution of code of practice complaints
About You
At least2-3yearsUK affiliateexperiencein theregulatory environment ofmaterial/copyreview, with a solid understanding ofABPI and IPHA Codes ofPractice
Confident reviewing and communicating complex scientific and clinical information in a clear, accurate, fairand balanced way
Enthusiastic, driven individualwith the ability towork autonomouslymanagingmultiple prioritiessimultaneously
Collaborative and open communicator who builds effective relationships across teams and functions
Proficient in the use of4M-PromoMatsand office tools, with astrongeye for detail when working with technical data
A degree in life sciences
Fluent in English
Why Choose Us
Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.
Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.
Help improve the lives of millions of people globally by making drug development quicker and more effective.
Enjoy opportunities to collaborate beyond your area of expertise, working with diverse teams across science, clinical, and digital fields to spark new ideas and drive breakthroughs.
Accelerate your professional development with structured career paths designed for both scientific and leadership advancement. Grow in ways you never imagined through bold moves that stretch your potential, cross moves into other business areas, and short-term gigs that build your scientific expertise.
Join a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice.
Achieve genuine work-life balance in a supportive R&D environment.
Enjoy outstanding benefits, including flexible working options, comprehensive healthcare, and well-being programs designed to help you thrive.
We are proud to be aDisability Confident Employer, committed to offering interviews to candidates who request consideration under the Scheme and meet the minimum requirements for this role.
If you have a disability and require adjustments for the interview process, please email us at diversity.recruitmentUKIE@sanofi.com. We are dedicated to ensuringan inclusiveand supportive experience for all applicants.
Visas for those who do not already have the right to work in the UK will be considered on acase by casebasis according to business needs and resources.
#LI-EUR
Pursue Progress. Discover Extraordinary.
Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.
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