Associate Director - Global Regulatory Affairs (Oncology Therapeutic Group)

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together. Find out more: Our approach to R&D   Position Summary : As Associate Director - Global Regulatory Affairs at GSK you will develop and execute global and regional regulatory strategies for oncology assets, ensuring optimal labelling and approvals while maintaining compliance with internal and external requirements. You will be accountable to the Global Regulatory Lead (GRL) and Global Regulatory Therapeutic Area (TA) Head and collaborate with cross-functional teams to shape development plans and regulatory interactions across multiple regions. We value clear thinking, collaboration, practical problem solving and a patient-first mindset. Responsibilities (include..,): ·       Work closely with GRL, global/regional counterparts and local operating companies to develop and deliver robust regulatory strategies that meet key market requirements. ·       Collaborate with cross-functional teams to align regulatory plans with Medicines Development Strategy and Integrated Asset Plan. ·       Support interactions, reviews, and submissions with regional/local regulatory authorities for product development and approval. ·       Assess regulatory intelligence, precedents and competitive landscape to inform strategy development and improve decision-making. ·       Ensure compliance with global, regional, and local regulatory requirements throughout the product lifecycle. ·       Drive process improvement, innovation, and performance excellence through the development and implementation of strategic changes. Location: This role is based in GSK HQ in London UK, Stevenage UK or alternatively in Switzerland Baar Onyx or Belgium - Wavre. The working pattern is hybrid, combining time in the office and remote work. Please Note – If the successful applicant is based at Stevenage site:  This role will temporarily be based at Stevenage.  However, the Company plans to relocate its offices to Cambridge, UK. The location of this role will therefore subsequently change to Cambridge UK, in accordance with timelines to be set by the Company.  The relocation is currently proposed to take effect by early 2029.     APPLICATION CLOSING DATE – Friday 30th of October 2026 (COB).   Basic Qualification: ·       Minimum: Bachelor’s degree in biological, pharmaceutical or healthcare science. ·       Proven experience in all phases of drug development in regulatory affairs and preferably in oncology. ·       Experience with clinical trial and licensing requirements in all major countries in the region and ideally knowledge of other key Agency processes globally ·       Experience leading regional development, submission and approval activities in local region(s). ·       Experience working effectively in matrix teams. ·       Strong written and verbal communication skills for clarity and impact ·       Strong experience of senior global stake-holder management.   Preferred Qualification : If you have the following characteristics, it would be a plus: ·       Advanced scientific degree (PhD, MD, PharmD). ·       Demonstrated ability to foster collaborative environments, proactively resolve challenges, and develop innovative solutions wi