Senior regulatory affairs officer Work, Jobs in Basingstoke, Ham (with Salaries)

Senior Regulatory Affairs Officer - Promotional & Non-Promotional Materials Review
Sanofi —Reading
- Hybrid work
- English
Senior Pharmacovigilance Officer, Team Lead/ Case Processing Manager- Medical Device experience needed
PrimeVigilance —Guildford
- Full-time
- Remote
- Nursing
- English
- Microsoft Office
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Senior Pharmacovigilance Officer, Team Lead/ Case Processing Manager- Medical Device experience needed
PrimeVigilance —Guildford
Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance.
Quick apply
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Senior Regulatory Affairs Officer - Promotional & Non-Promotional Materials Review

Sanofi -
Reading

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Job details

Qualifications

English

Full job description

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 experience in the regulatory environment of material/copy review, with a solid understanding of ABPI and IPHA Codes of Practice

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 managing 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 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 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

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senior regulatory affairs officer jobs in basingstoke, ham

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

Senior Pharmacovigilance Officer, Team Lead/ Case Processing Manager- Medical Device experience needed

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