Senior Manager, Regulatory Affairs (Consultant)Location: Maidenhead/Remote (hybrid)Duration: 6 months initialRate: £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 ResponsibilitiesLead the development and implementation of regulatory strategies and risk assessments for assigned products across the Europe AreaRepresent regional regulatory requirements within global regulatory project teams to ensure appropriate consideration in global strategyCollaborate with affiliate Regulatory Affairs teams to guide submissions, health authority interactions and lifecycle management activitiesAssess scientific data for regulatory submissions, identify gaps, and develop mitigation strategies to support approvalsMonitor evolving European legislation and lead the development of regulatory responses and policy implementationSkills & Experience RequiredDegree in pharmacy, biology, chemistry, pharmacology, or related life sciences disciplineStrong experience in European Regulatory Affairs, including centralised, MRP/DCP and national proceduresProven track record leading regulatory activities for development products (e.g., scientific advice, PIP) Effective communicator able to work across complex international and matrixed environmentsStrong leadership, organisational skills and ability to work independently with minimal supervisionTo apply:SRG would be delighted to discuss this opportunity further with you. Please click to apply or contact Theo Charles for more details.