Vice President, Global Regulatory Affairs Strategy

<div><h3>Overview</h3><p><strong>Site Name:</strong> USA - Pennsylvania - Upper Providence, GSK HQ, USA - Massachusetts - Cambridge, Wavre</p><p><strong>Posted Date:</strong> Jan 28 2026</p><p><strong>Business Introduction</strong></p><p>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.</p><p>Find out more: Our approach to R&D</p><h3>Position Summary</h3><p>In this critical leadership role, the VP Global Regulatory Strategy RI&I will oversee regulatory strategy globally for the RI&I portfolio, including the associated communication strategy to all regulatory authorities. Moreover, the VP will act as a direct link between Regulatory Affairs and all RI&I R&D stakeholders and provide the regulatory input to Governance decisions for clinical/project regulatory matters. They will also serve as a senior leader and the responsible head who ensures appropriate regulatory compliance in the conduct of global development programs and product lifecycle maintenance and license to operate activities for the RI&I portfolio. This role will be a member of the Global Regulatory Strategy LT as well as leading the GRS RI&I team of approximately 60 FTEs.</p><h3>Key Responsibilities</h3><ul><li>Directly accountable for global regulatory development and filings for the RI&I portfolio of products.</li><li>Ensures that sound regulatory practices are fully integrated into pre-clinical, clinical and technical submissions, and that all documents submitted to regulatory agencies are appropriately reviewed to ascertain they are complete, scientifically accurate, of high quality, in regulatory compliance and presented in a manner that facilitates agency review.</li><li>Contributes to the creation and implementation of development plans that incorporate regulatory strategies designed to maximise the likelihood of successful regulatory applications, delivering regulatory approval, key labeling claims and reimbursement for all key indications.</li><li>Exhibits leadership in the formulation and execution of global regulatory strategies and contributes to the development and implementation of policies and strategies for optimisation of development, lifecycle maintenance and license to operate.</li><li>Monitors and anticipates regulatory, scientific and pertinent legal issues and assesses potential impact on GSK; advises senior management on events of significance to GSK’s business interests; proactively influences changes in guidelines and regulation to strengthen the regulatory review process and ensure core operations are proactively aligned with emerging policies.</li><li>Develops and maintains excellent working relationships with FDA, EMA, PMDA and CFDA and other key international regulatory agencies, overseeing the planning and implementation of agency meetings, as appropriate; assuring collaborative approaches to product development and clinical plans with agencies via scientific advice and protocol assessment procedures.</li><li>Provides leadership to assure appropriate regulatory compliance in the conduct and reporting of clinical trials, institutionalise policies and procedures and track performance.</li><li>Attracts, develops and retains key regulatory professionals, recognised for their strategic focus and regulatory and scientific acumen in alignment with the principles of Project First, Expert Led, and Tech Enabled.</li><li>Represents Global Regulatory Affairs for RI&I on senior level decision making bodies.</li><li>Acts as a credible, influential, respected spokesperson during interactions with international regulatory agencies and external organisations, and ensures appropriate, proactive communication with agencies to assure expedient and efficient review and approval of submissions.</li><li>Serves as an external proactive industry leader and influential spokesperson in support of GSK enterprise priorities and regulatory initiatives, and in shaping the external environment.</li><li>Serves as the senior regulatory input to RI&I R&D stakeholders and senior level governance boards.</li><li>Drives the