Clinical supply chain manager

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. Position Summary You will lead end‑to‑end clinical supply planning and delivery for assigned investigational assets. You will work closely with clinical teams, quality, regulatory and external partners to design patient‑focused, risk‑adjusted supply strategies. Your role will influence clinical decisions, manage risks, and ensure timely delivery of clinical trial materials. We value clear communicators, curious problem‑solvers, and people who collaborate with respect and accountability. This role offers growth, real impact on patient studies, and alignment with GSK’s mission of uniting science, technology and talent to get ahead of disease together. This role can report into DDS‑CM&SC‑Global Supply Chain Planning‑ID‑Vaccines (Mark Landau), DDS‑CM&SC‑Global Supply Chain Planning‑R‑II HIV (Aurelie Hanoteau), or DDS‑CM&SC‑Global Supply Chain Planning‑Oncology (Colin Shelton). Responsibilities Lead cross‑functional supply planning for clinical programs from protocol to patient delivery. Create and maintain demand and supply plans, including inventory policy and contingency scenarios. Manage clinical packaging, labeling, and distribution activities with internal and external partners. Oversee Interactive Response Technology (IRT) specifications, testing and maintenance to support randomization and supply control. Proactively identify supply risks and lead mitigation activities to ensure continuity and patient delivery. Track program costs, manage budgets and supplier contracts, and report status to stakeholders. Basic Qualification Bachelor’s degree in pharmacy, chemistry, life sciences, logistics, supply chain or related field. 3+ years’ experience in clinical supply chain or clinical trial materials planning and execution. Experience with clinical packaging, labeling, distribution and inventory management. Experience supporting IRT systems or other randomization/inventory management tools. Working knowledge of relevant quality and regulatory expectations (c GMP, GCP, ICH, or equivalent). Experience working with cross‑functional teams and effectively communicating supply constraints and possible solutions to clinical and project leadership. Preferred Qualification Master’s degree in a relevant discipline or additional supply chain certification. 5+ years’ experience in pharmaceutical clinical supply chain or pharmaceutical industry experience. Experience with global import/export logistics, temperature‑controlled shipments and cold chain management. Experience creating technical agreements, packaging specs and batch record review. Strong project management skills, including managing timelines, budgets and suppliers. Experience influencing program decisions and leading cross‑functional teams in a matrix environment. Salary and Benefits Italian Salary Range: EUR 0 to EUR 0 Belgium Salary Range: EUR 80,250 to EUR 133,750 The 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. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at usrecruitment.adjustments@. Equal Opportunity Statement GSK is an Equal Opportunity Employer. This ensures that 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 (including family medical history), military service or any basis prohibited under federal, state or local law. #J-18808-Ljbffr