At a Glance
- Tasks: Lead the review of promotional materials, ensuring compliance with legal standards and industry codes.
- Company: Join Sanofi, a pioneering biopharma company at the forefront of drug discovery.
- Benefits: Flexible working options, comprehensive healthcare, and a supportive work-life balance.
- Other info: Diverse and inclusive workplace with excellent career growth opportunities.
- Why this job: Make a real impact on global health by improving drug development processes.
- Qualifications: 2-3 years in regulatory affairs with strong communication skills and a life sciences degree.
The predicted salary is between 46000 - 52000 € per year.
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.
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 diversity.recruitmentUKIE@sanofi.com. 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.
Senior Regulatory Affairs Officer employer: Sanofi
Sanofi is an exceptional employer that champions innovation and collaboration in the biopharma sector, offering a dynamic work environment in Reading, UK. With a strong commitment to employee growth, you will have access to structured career paths, diverse team collaborations, and a culture that prioritises diversity, equity, and inclusion. Enjoy flexible working arrangements, comprehensive healthcare benefits, and a supportive atmosphere that fosters work-life balance while making a meaningful impact on global health.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Regulatory Affairs Officer
✨Tip Number 1
Network like a pro! Reach out to current or former employees at Sanofi on LinkedIn. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of ABPI and IPHA Codes of Practice. Be ready to discuss how you've navigated regulatory challenges in the past—show them you're the expert they need!
✨Tip Number 3
Practice your communication skills! You’ll need to explain complex scientific info clearly. Try explaining a tricky concept to a friend or family member to get comfortable with it.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re serious about joining the team at Sanofi.
We think you need these skills to ace Senior Regulatory Affairs Officer
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the Senior Regulatory Affairs Officer role. Highlight your experience with promotional and non-promotional materials, and show how you meet the specific requirements mentioned in the job description.
Showcase Your Skills:Don’t just list your qualifications; demonstrate how your skills align with the responsibilities of the role. Use examples from your past experiences to illustrate your understanding of regulatory processes and compliance requirements.
Be Clear and Concise:When writing your application, keep it straightforward and to the point. Use clear language to communicate your thoughts, especially when discussing complex scientific information. Remember, clarity is key in regulatory affairs!
Apply Through Our Website:We encourage you to apply directly through our website. This ensures your application gets to the right people and helps us keep track of all candidates efficiently. Plus, it’s super easy to do!
How to prepare for a job interview at Sanofi
✨Know Your Regulatory Stuff
Make sure you brush up on the ABPI and IPHA Codes of Practice. Being able to discuss these in detail will show that you’re not just familiar with them, but that you can apply them in real-world scenarios. Prepare examples of how you've navigated compliance challenges in your previous roles.
✨Showcase Your Communication Skills
As a Senior Regulatory Affairs Officer, you'll need to communicate complex scientific information clearly. Practice explaining technical concepts in simple terms, as this will be crucial when working with marketing and medical teams. Consider role-playing with a friend to refine your delivery.
✨Build Relationships Before You Even Start
Think about how you can foster strong working relationships with potential colleagues. Research the team structure and be ready to discuss how you would collaborate with different departments. Mention any past experiences where you successfully built rapport with cross-functional teams.
✨Prepare for Scenario Questions
Expect to face scenario-based questions during your interview. Think about potential challenges you might encounter in the role and how you would address them. Prepare specific examples from your experience that demonstrate your problem-solving skills and ability to balance innovation with regulatory requirements.
