Site Name: USA - Pennsylvania - Upper Providence, UK - Hertfordshire - StevenagePosted Date: May 5 2026 At GSK, the Clinical Manufacturing & Supply Chain (CMSC) organization is responsible for the enterprise-wide delivery of GMP clinical manufacturing for the small and large molecule medicines pipeline, and cross-modality clinical supply chain management, labelling, packaging and distribution for the R&D vaccines and medicines. The Clinical Supply Systems function within CMSC is dedicated to deploying and supporting innovative digital technologies and systems that advance clinical supply chain management by maintaining the current systems roadmap and ensuring modernization aligns with business strategy to drive automation, leverage data for enhanced insights, and improve overall efficiency. Position Summary: Provide leadership for a team of business professionals in the development, deployment, support, and maintenance of key IT systems used in the R&D clinical supply chain. You will work closely with clinical operations, supply planning, manufacturing, quality, IT and external partners, acting as a bridge between business objectives and system capabilities to ensure measurable outcomes and alignment with enterprise priorities and R&D objectives. Responsibilities Ensure systems are developed, deployed, supported, and maintained in accordance with GSK policies & procedures. Ensure systems and supporting documentation are maintained in a constant state of inspection readiness. Ensure team members are adequately trained and are performing effectively in developing, deploying, supporting, and maintaining systems. Ensure these systems remain aligned to current business strategies and regulatory requirements. Provide effective leadership in support of quality deviations & investigations and system outages. Develop effective networks with GSK R&D Tech and system vendors. Escalate system risks when identified and ensure EHS risks are identified and mitigated. Manage budget, people, technical activities, health & safety, GMP, and other specific responsibilities inherent to the role. Basic Qualifications Degree in Computer Science, Engineering, data engineering, or a related field. 8+ years of experience in product management, system access with 6+ years in the pharmaceutical industry or supply chain management. Relevant pharmaceutical/biotech or similar industry experience. 5+ years of operational experience with the R&D clinical supply chain in technologies such as Signant Health Systems: PMD/SSF/SSP, RTSM, SAP/ERP, Veeva CTMS. 8+ years of professional experience in Product Ownership or Product Management. Proficiency with Jira/Confluence and AHA. Experience developing, deploying, supporting, and maintaining IT systems in a regulated environment. Experience managing external vendors. Preferred Qualifications Advanced degree in supply chain, engineering, life sciences, business or a related discipline. Hands‑on experience with clinical supply platforms, warehouse management systems or serialization solutions. Deep knowledge of supply chain systems data models and business contexts. Experience managing vendors and contracts for outsourced supply or technology services. Knowledge of global clinical supply regulations and good distribution practices. Practical skills in data analytics, dashboards or BI tools to drive improvements. Comfortable working in hybrid environments with distributed teams and flexible collaboration. Proven ability to lead and influence teams without direct authority. Location and Working Model This role is based in the United States and is hybrid, requiring an on‑site presence approximately 2–3 days per week. Flexibility options will be discussed during the hiring process. GSK is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity and sexual orientation), parental status, national origin, age, disability, genetic information (family medical history), military service or any basis prohibited under federal, state or local law. #J-18808-Ljbffr