Manager, Supply Chain

Job Responsibilities Interpret clinical study protocols and/or dosing schema; translate to IMP demand/supply planning and distribution strategies, including depot inventory management. Perform demand and/or supply forecasting and planning (9–18 month horizon); translate forecasts into clinical packaging and labeling (CPL) execution plans; support contract/quote reviews and purchase order/invoice reconciliations. Develop and implement depot and clinical site seeding and resupply strategies. Execute operational/logistics strategies with Quality Assurance and other functional groups to ensure on‑time, safe delivery of all clinical shipments. Collaborate with Logistics, GCSC, PDM, and external partners to resolve shipping issues; escape to senior leadership as needed. Support clinical development and PDM strategies; develop clinical supply strategies and plans focused on compliant, quality IMP delivery globally on time in full. Ensure accurate inventory and depot records through timely reconciliation. Track clinical supply incidents/issues; report, escape, and investigate root cause as appropriate. Perform tasks in Gilead systems (e.g., SAP, IVRS, QMS) to enable compliant IMP progression through the supply chain. Author SOPs and business process work instructions as directed. Support regulatory filings and inspections. Maintain compliance of clinical supply deliverables for CSR and TMF. Monitor shipment‑related incidents and quality trends; assist in CAPAs. Maintain GDP, GMP, global trade compliance; maintain required training compliance. Obtain/review quotes; approve purchase requisitions and invoices. Basic Qualifications Bachelor’s degree + 6+ years industry experience OR Master’s degree + 4+ years OR PhD/PharmD + 0+ years. Sciences degree preferred. Preferred Qualifications Strong clinical supply management knowledge (forecasting, demand/supply planning, distribution strategies, IVRS and ERP). Knowledge of clinical study designs, blinding practices, and global trials (Phase 1 to late phase). Knowledge of Clinical Demand and Operations Planning (CD&OP). Experience managing comparator drugs and other co‑meds. Ability to collaborate/influence/negotiate with cross‑functional teams and external suppliers. Works effectively with ambiguity; devises/implements best options aligned to values. Excellent verbal, written, interpersonal communication; clear, concise documents/presentations. Strong computer skills; ability to adopt Gilead systems/databases. Ability to manage resources and timelines for complex clinical studies/programs (project management a plus). Benefits Company‑sponsored medical, dental, vision, and life insurance plans; paid time off; discretionary annual bonus and discretionary stock‑based long‑term incentives (eligibility may vary). Application Instructions For current Gilead employees and contractors: apply via the Internal Career Opportunities portal in Workday. #J-18808-Ljbffr Scorpion Therapeutics