Zenopa are working with a global pharma company with differentiated medicines in oncology, immunology, infectious diseases, ophthalmology and diseases of the central nervous system. As a Regulatory Partner, you will be a vital part of our UK Regulatory Chapter. You will leverage your regulatory and scientific expertise to shape and drive strategic initiatives. This is your opportunity to make a difference and be part of a company dedicated to improving lives. Our activities encompass:Clinical Trial ApplicationsNational Licensing ApplicationsEarly Access to Medicines ApplicationsNational components of medicines authorization via the European Centralized procedureThe team serves as the primary contact with the MHRA, requiring effective cross-functional collaboration at both local and global levels, as well as the capability to negotiate and influence externally. Regulatory Partners need to be adaptable and entrepreneurial to identify opportunities, while maintaining a focused approach on ensuring compliance and playing a key role in retaining the UK''s License to Operate.Experience Required:A Scientific University degreeExtensive experience in UK Regulatory AffairsProven experience managing UK submissions post-BrexitExperience providing strategic and technical adviceA proven track record of developing, implementing, and communicating regulatory strategiesExperience in mentoring peers, as well as managing stakeholder ..... full job details .....