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 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.