Manager, Supply Chain

Job Responsibilities Interpret clinical study protocols and/or dosing schema; translate into IMP demand/supply planning requirements 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 management, GCSC, PDM, and external partners to resolve shipping issues; elevate to senior leadership as needed. Support clinical development and PDM strategies to develop clinical supply strategies and plans focused on delivering compliant, quality IMP globally on time in full. Ensure accurate depot inventory and records through timely reconciliation. Monitor clinical supply incidents/issues; report/escalate and investigate root cause as appropriate. Use 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. Assist with CAPAs; maintain GDP/GMP/global trade compliance and required training. 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 experience (forecasting, demand/supply planning, distribution strategies, IVRS, ERP). Clinical study design and blinding practices; global trials (Phase 1 first-in-human 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; strong communication skills. Strong computer skills and ability to adopt systems/databases. Ability to manage resources/timelines for complex studies/programs; project management a plus. #J-18808-Ljbffr Scorpion Therapeutics