Company TMC Pharma Services Ltd, based in Hartley Wintney, provides expert support services to the pharmaceutical industry with a focus on drug development, regulatory affairs, consultancy, and post-approval/marketing support. The team excels in delivering successful projects and thrives on tackling unique challenges. TMC collaborates with clients ranging from biotech start-ups to multinational corporations in Europe, the USA, and worldwide. Role Summary This is a full-time hybrid role for a Director of Regulatory Affairs at TMC Pharma Services Ltd. The Director will be responsible for leading regulatory strategy development, overseeing regulatory submissions, and providing cross-functional team leadership. While the role is based in Hartley Wintney, there is flexibility for remote work. Skills and Experience- required Life cycle maintenance of CP licences - additional experience in national, MRP, DCP licences welcomed. IND compilation Preparation of Module 1 documents Able to provide strategic leadership during product development from early stages to MAA. Coordination of regulatory procedures such as ODDs, PIPs, scientific advice, PRIME etc. Coordination of MAAs including pre-submission activities, Rapporteur meetings, oversight of dossier preparation and submission. Preferred: Ability to author clinical, CMC, or non-clinical documents/modules preferred US regulatory experience useful