Senior Regulatory Affairs Officer - Promotional & Non-Promotional Materials Review

Job Title: Senior Regulatory Affairs Officer - Promotional & Non-Promotional Materials Review 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 promotional and non-promotional review 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 constructive comments and feedback to 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 with key stakeholders to 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 least 2-3 years UK affiliate e xperience in the regulatory environment of material /copy review , with a solid understanding of ABPI and IPHA C odes of P ractice Confident reviewing and communicating complex scientific and clinical information in a clear, accurate , fair and balanced way Enthusiastic, driven individual with the ability to work autonomously manag ing multiple priorities simultaneously Collaborative and open communicator who builds effective relationships across teams and functions Proficient in the use of 4M-PromoMats and office tools, with a strong eye for detail when working with technical data A degree in life science s 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 a Disability 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 [email protected]. We are dedicated to ensuring an inclusive and supportive experience for all applicants. Visas for those who do not already have the right to work in the UK will be considered on a case by case basis according to business needs and resources. #LI-EUR Pursue progress , discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !