Senior Regulatory Affairs Officer
Reading, 英国 Regular 发布于 May. 21, 2026 申请截止于 Jun. 09, 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
追寻 发展。探索 菲凡。
进步需要我们每个人的参与——不论其背景、地域、或职业,我们都有一个共同的愿望:创造奇迹。你也可以成为其中的一员。我们不断追求变革,拥抱新思想,探索我们所能提供的一切机会。让我们一起追求进步。共同发现非凡。
在赛诺菲,不分种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾或性别认同,我们为所有人提供平等的机会。
观看 “在赛诺菲的一天” ,并在官网 (sanofi.com) 上查看赛诺菲的多元化、公平与包容倡议!
体验可能性
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Innovation in Action
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Sustainable and Green
Our new facility was built to minimize the environmental impact — helping protect our planet and people. Using resources efficiently, we're providing greener, healthier workspaces.
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心怀梦想,成就一番事业
我们希望您以饱满的热情投入到自己的工作岗位中,给全球数百万人带来美好生活。您的职业发展道路由您自己来掌控。您只管制定目标,我们会提供充足的培训机会和支持,让您得偿所愿。
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我们的故事
我们关注每一个员工的声音。因为,我们的未来取决于所有员工的付出与努力。正因为他们的助力,我们才能追求远大的理想。