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Sanofi logo
赛诺菲
Senior Regulatory Affairs Officer - Promotional & Non-Promotional Materials Review
立即应聘

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

发布于 大约 7 小时前

普通员工/个人贡献者

Reading, United Kingdom
中级经验
全职员工
混合式弹性办公
本科
法务、风险与合规
mentoring
Cross-Functional Collaboration
Compliance
Regulatory Affairs
4M-Promomats
Abpi
Ipha
Material Review

AI 估算 · 30k–45k

Senior Regulatory Affairs role in UK pharma, typical salary range £40k-£60k per annum, converted to RMB at mid-rate.

职位详情

关于这个职位

This role focuses on ensuring that promotional and non-promotional materials for Sanofi's diverse portfolio comply with UK regulations and industry codes. You will review materials, provide regulatory advice to cross-functional teams, and mentor junior colleagues. It offers a blend of independent work and collaboration within a leading biopharma company.

最低要求

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. Enthusiastic, driven individual with ability to work autonomously managing multiple priorities. Collaborative and open communicator. Proficient in 4M-PromoMats and office tools. A degree in life sciences. Fluent in English.

工作职责

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.

AI 洞察

优缺点分析

优点

  • Join a global biopharma leader with a strong pipeline and commitment to innovation, including AI-powered research.
  • Gain deep expertise in UK regulatory frameworks and codes, making you a highly valued specialist.
  • Enjoy flexible working (3 days onsite, 2 remote) and a supportive work-life balance culture.
  • Opportunities for structured career growth, mentoring, and cross-functional exposure.
  • High level of responsibility for ensuring compliance, with potential pressure from tight review timelines.
  • Need to stay updated with evolving regulations and codes, requiring continuous learning.
  • Balancing innovation with regulatory constraints can be demanding.
  • This role is ideal for an experienced regulatory professional with a life sciences background who thrives on meticulous review and enjoys collaborating with diverse teams to ensure high-quality, compliant materials.

缺点 / 挑战

暂无明显挑战项

角色解读

  • Advance to Regulatory Affairs Manager, leading a team and overseeing broader compliance activities.
  • Move into strategic roles within Regulatory Affairs or transition to medical affairs roles leveraging regulatory expertise.
  • Opportunities for cross-functional moves into commercial or R&D roles within the company.
  • Review promotional and non-promotional materials to ensure compliance with ABPI and IPHA codes and legal requirements.
  • Provide expert regulatory advice to marketing, medical, and governance teams, supporting brand planning and material development.
  • Mentor and coach team members on regulatory processes and best practices.
  • Lead projects and deliver training to internal stakeholders on material review systems.
  • In-depth knowledge of ABPI and IPHA Codes of Practice and UK regulatory environment.
  • Strong analytical and communication skills to evaluate and convey complex scientific information.
  • Proficiency with 4M-PromoMats or similar material review systems.
  • Ability to manage multiple priorities autonomously and collaborate across teams.

申请策略

  • Tailor your CV to plainly state your UK regulatory experience and familiarity with relevant codes.
  • Research Sanofi's pipeline and therapeutic areas to show genuine interest.
  • Prepare to discuss how you handle conflicting priorities and regulatory challenges.
  • Emphasize your experience with UK material review and deep understanding of ABPI/IPHA codes.
  • Highlight specific examples of complex reviews you've led or improved processes.
  • Showcase your ability to work cross-functionally and mentor junior staff.
  • Demonstrate proficiency with 4M-PromoMats or similar systems.
  • Deepen your knowledge of the latest ABPI code updates and industry best practices.

面试指南

  • Use the STAR method (Situation, Task, Action, Result) for behavioral questions to structure your response.
  • For regulatory scenarios, clearly state the requirement, your analysis, and the outcome, emphasizing patient safety and compliance.
  • Demonstrate your ability to balance business needs with regulatory obligations by showing pragmatic solutions.
  • Can you describe a time you identified a compliance issue in promotional materials and how you resolved it?
  • How do you stay updated with changes in the ABPI or IPHA codes?
  • Tell me about a challenging cross-functional collaboration and how you ensured regulatory alignment.
  • How would you handle a situation where a marketing team disagrees with your regulatory feedback?
  • Describe your experience with 4M-PromoMats or similar material review systems.

职位点评

80
综合评分

Senior regulatory specialist role at a top biopharma with hybrid flexibility, strong development opportunities, and meaningful impact.

更适合这类人
This role is best suited for a regulatory professional who prioritizes skill growth, work-life balance, and purpose-driven work, and who is comfortable with moderate salary certainty.
表现最好
成长发展
相对薄弱
薪资福利
薪资福利75
成长发展85
工作生活80
使命价值80

薪资福利

75中等

Salary not disclosed but typical for senior regulatory roles at large pharma; comprehensive benefits package including flexible working, healthcare, and well-being programs.

薪资信号未披露(AI估算:30K-45K/月)
福利待遇flexible working options、comprehensive healthcare、well-being programs

成长发展

85较高

Strong growth signals with structured career paths, mentoring opportunities, and cross-functional collaboration. Position offers leadership development and skill enhancement.

技术前沿传统/成熟技术
技术栈Regulatory Affairs、ABPI、IPHA、4M-PromoMats
成长机会structured career paths、mentoring、cross moves
业务类型ambiguous

工作生活

80较高

Hybrid working model (3 days onsite, 2 remote) and explicit emphasis on work-life balance. Office location in Reading (commutable from London and other areas).

工作模式混合式弹性办公 (2 days remote per week)
办公地点未明确
加班情况明确说明WLB/不加班
工作生活平衡work-life balance、flexible working options

使命价值

80较高

Role contributes to improving patients' lives through ensuring safe and accurate promotional materials. Company mission emphasizes scientific progress and patient impact.

行业发展稳定成熟行业
社会影响正向社会影响力较高
使命信号improve people's lives、chase the miracles of science
创新程度积极采用新技术
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  • 浏览职位
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  • 数据方法论
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  • 免费试用
  • 价格方案
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© 2026 Watch Jobs. 保留所有权利

Created by jianglicat - 讲礼猫

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