Supply Chain Manager, CMSC WSL

Responsibilities

• This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
• 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.
• Why You?
• Basic Qualification
• We are seeking professionals with the following required skills and qualifications to help us achieve our goals
• 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 (cGMP, GCP, ICH, or equivalent).
• E xperience working with cross-functional teams and effectively communicating supply constraints and possible solutions to clinical and project leadership.
• Preferred Qualification
• If you have the following characteristics, it would be a plus
• 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.
• #LI-GSK

Benefits

Additional Information

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 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)

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