Associate Director

pAt 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 RD 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. /p pFind out more: /p pOur approach to RD /p h3Position Summary /h3 pAs 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. /p h3Responsibilities (include..,): /h3 ulliWork closely with GRL, global/regional counterparts and local operating companies to develop and deliver robust regulatory strategies that meet key market requirements. /liliCollaborate with cross-functional teams to align regulatory plans with Medicines Development Strategy and Integrated Asset Plan. /liliSupport interactions, reviews, and submissions with regional/local regulatory authorities for product development and approval. /liliAssess regulatory intelligence, precedents and competitive landscape to inform strategy development and improve decision-making. /liliEnsure compliance with global, regional, and local regulatory requirements throughout the product lifecycle. /liliDrive process improvement, innovation, and performance excellence through the development and implementation of strategic changes. /li /ul h3Location: /h3 pThis 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. /p pPlease 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. /p h3APPLICATION CLOSING DATE – Friday 30th of October 2026 (COB). /h3 h3Basic Qualification: /h3 ulliMinimum: Bachelor’s degree in biological, pharmaceutical or healthcare science. /liliProven experience in all phases of drug development in regulatory affairs and preferably in oncology. /liliExperience with clinical trial and licensing requirements in all major countries in the region and ideally knowledge of other key Agency processes globally /liliExperience leading regional development, submission and approval activities in local region(s). /liliExperience working effectively in matrix teams. /liliStrong written and verbal communication skills for clarity and impact /liliStrong experience of senior global stake-holder management. /li /ul h3Preferred Qualification /h3 pIf you have the following characteristics, it would be a plus: /p ulliAdvanced scientific degree (PhD, MD, PharmD). /liliDemonstrated ability to foster collaborative environments, proactively resolve challenges, and develop innovative solutions within regulatory constraints. /liliProficiency in digital fluency tools to enhance project delivery, efficiency, and innovation. /li /ul h3Skills /h3 pBusiness Resilience, Communication, Digital Fluency, Matrix Leadership, Pharmaceutical Regulatory Compliance, Regulatory Strategies, Resource Management, Stakeholder Management /p h3Belgium Salary Range / Fourchette salariale – Belgique: EUR 98,250 to EUR 163,750 /h3 pThe annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process. This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown. Salary ranges for other locations are shown because some markets have pay transparency laws that require