
普通员工/个人贡献者
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.
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.
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.
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.
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Senior regulatory specialist role at a top biopharma with hybrid flexibility, strong development opportunities, and meaningful impact.
Salary not disclosed but typical for senior regulatory roles at large pharma; comprehensive benefits package including flexible working, healthcare, and well-being programs.
Strong growth signals with structured career paths, mentoring opportunities, and cross-functional collaboration. Position offers leadership development and skill enhancement.
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).
Role contributes to improving patients' lives through ensuring safe and accurate promotional materials. Company mission emphasizes scientific progress and patient impact.