Senior Manager, Regulatory Affairs (Consultant)
Location: Maidenhead/Remote (hybrid)
Duration: 6 months initial
Rate: £70-85 per hour (based on experience)
We are working with a leading pharmaceutical company who are seeking an experienced Senior Manager, Regulatory Affairs to shape and drive regulatory strategy across the Europe Area. This high‑impact role will work across development and marketed products, partnering closely with global teams, affiliates and health authorities to ensure successful regulatory outcomes.
Key Responsibilities
* Lead the development and implementation of regulatory strategies and risk assessments for assigned products across the Europe Area
* Represent regional regulatory requirements within global regulatory project teams to ensure appropriate consideration in global strategy
* Collaborate with affiliate Regulatory Affairs teams to guide submissions, health authority interactions and life‑cycle management activities
* Assess scientific data for regulatory submissions, identify gaps, and develop mitigation strategies to support approvals
* Monitor evolving European legislation and lead the development of regulatory responses and policy implementation
Skills & Experience Required
* Degree in pharmacy, biology, chemistry, pharmacology, or related life sciences discipline
* Strong experience in European Regulatory Affairs, including centralised, MRP/DCP and national procedures
* Proven track record leading regulatory activities for development products (e.g., scientific advice, PIP)
* Effective communicator able to work across complex international and matrixed environments
* Strong leadership, organisational skills and ability to work independently with minimal supervision
To apply
SRG would be delighted to discuss this opportunity further with you. Please click to apply or contact Theo Charles for more details.
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