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- Tasks: Review promotional and non-promotional materials while ensuring compliance with legal standards.
- Company: Join an innovative global healthcare company dedicated to improving lives through science.
- Benefits: Enjoy a comprehensive rewards package, health benefits, and flexible career growth opportunities.
- Why this job: Be part of a supportive team that values your contributions and fosters professional development.
- Qualifications: Degree in a scientific discipline or relevant regulatory experience; strong communication skills required.
- Other info: Visa sponsorship considered; equal opportunity employer.
The predicted salary is between 36000 - 60000 £ per year.
Regulatory Affairs Officer – Promotional & Non-promotional Materials Review
Location: Reading, UK
About the job
With this exciting opportunity within Regulatory Affairs, you will be responsible for the provision of high-quality promotional and non-promotional review services to internal stakeholders, which conform to all relevant legal requirements, ABPI & IPHA Codes of Practice, company guidelines and policies.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main responsibilities:
- Promotional and non-promotional materials review and internal stakeholder support
- Requirement for full compliance with company procedures, ABPI and IPHA Codes of Practice, and industry guidance.
- Establish and cultivate a good working relationship with internal customers such as Commercial, Medical and Medical Governance colleagues to ensure that the services provided are relevant to the business needs.
- To complete Regulatory Review and scientific accuracy of Sanofi marketed/pre-launch products and related disease area materials to ensure they comply with the relevant UK and Irish Codes of Practice and Sanofi policies.
- Attend brand planning and strategy discussions/meetings to provide regulatory material review input.
- Respond to internal enquiries in relation to the material review process/good material review practice in a timely and effective manner.
- Highlight potential issues with materials at the conceptual stage of development.
- Lead or participate in team projects.
- Maintenance of information resources
- Produce and update Prescribing Information related to promoted products.
About you:
- Degree educated with a scientific discipline (or equivalent) or proven relevant experience within the regulatory environment.
- Competent in the use of PromoMats is desirable but not a requirement.
- Excellent written and verbal communication skills and interpersonal skills.
- An ability to understand, analyse and communicate relatively complex pharmacy, pharmacological, and clinical information about Sanofi products in a systematic, fair and balanced way.
- Accuracy and an eye for detail working with technical clinical data and material review. Able to prioritise with the appropriate sense of urgency based on customers’ and business needs; excellent time management skills.
- Application of sound professional judgement to ethical issues and make appropriate informed decisions without supervision.
- Able to quickly pick-up on new therapy areas and disseminate information in a clear and accurate manner.
- Ability to work under pressure, independently and as part of a team, in an open and professional manner, delivering high-quality work to meet timelines.
- Demonstrate the ability to interact professionally with key experts, negotiate on content and make constructive suggestions.
Why choose us?
- Bring the miracles of science to life alongside a supportive, future-focused team.
- Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
- Enjoy a thoughtful, well-crafted rewards package that recognises your contribution and amplifies your impact.
- Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
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.
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.
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Regulatory Affairs Officer - Promotional & Non-promotional Materials Review employer: Sanofi
Contact Detail:
Sanofi Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Officer - Promotional & Non-promotional Materials Review
✨Tip Number 1
Familiarize yourself with the ABPI and IPHA Codes of Practice. Understanding these guidelines will not only help you in your role but also demonstrate your commitment to compliance during interviews.
✨Tip Number 2
Network with professionals in the regulatory affairs field. Attend industry events or webinars to connect with potential colleagues and learn more about the current trends and challenges in regulatory review.
✨Tip Number 3
Showcase your ability to handle complex information by preparing examples of past experiences where you successfully navigated regulatory challenges. This will highlight your analytical skills and attention to detail.
✨Tip Number 4
Demonstrate your communication skills by practicing how to explain complex clinical data in simple terms. This is crucial for collaborating with internal stakeholders and ensuring everyone is on the same page.
We think you need these skills to ace Regulatory Affairs Officer - Promotional & Non-promotional Materials Review
Some tips for your application 🫡
Understand the Role: Make sure you fully understand the responsibilities of a Regulatory Affairs Officer. Familiarize yourself with the ABPI & IPHA Codes of Practice and how they apply to promotional and non-promotional materials.
Tailor Your CV: Highlight your relevant experience in regulatory affairs, especially any work related to promotional materials. Emphasize your scientific background and any specific skills that align with the job description.
Craft a Strong Cover Letter: In your cover letter, express your passion for regulatory affairs and how your skills can contribute to the company's mission. Mention your ability to communicate complex information clearly and your experience working with internal stakeholders.
Proofread Your Application: Before submitting, carefully proofread your application for any errors. Ensure that your writing is clear, concise, and free of jargon, as attention to detail is crucial in this role.
How to prepare for a job interview at Sanofi
✨Understand Regulatory Requirements
Make sure you are well-versed in the ABPI and IPHA Codes of Practice, as well as any relevant legal requirements. Being able to discuss these regulations confidently will show your understanding of the role's responsibilities.
✨Showcase Your Communication Skills
Since the role involves interacting with various internal stakeholders, be prepared to demonstrate your excellent written and verbal communication skills. Share examples of how you've effectively communicated complex information in the past.
✨Highlight Attention to Detail
Given the importance of accuracy in reviewing promotional and non-promotional materials, be ready to discuss your experience with technical data and how you ensure precision in your work.
✨Demonstrate Team Collaboration
The ability to work under pressure and as part of a team is crucial. Prepare to share instances where you've successfully collaborated with others, especially in high-stakes situations or projects.
