Manager, Clinical Supply Chain - Planning

Responsibilities Build and maintain clinical supply forecasts by translating protocol assumptions (enrollment rates, dosing schedules, country footprint) into study‑level demand; continuously update as trials progress. Develop integrated CFG supply plans aligning forecasted demand with inventory strategy to ensure adequate supply while minimizing overage, expiry risk, and waste. Anticipate and quantify future supply risks (assumptions, scenarios, constraints) and recommend mitigations/tradeoffs before they impact trial continuity. Collaborate with Global Planning and CMC to translate demand forecasts into manufacturing, packaging, and release plans, aligned on lead times, capacity constraints, and material availability. Validate and refine forecasting assumptions with Program Development/Clinical Teams as study designs, enrollment dynamics, and protocols evolve. Partner with Finance to connect demand forecasts to long‑range budget planning and scenario modeling. Qualifications B.Sc. in a scientific field, Supply Chain Management, or related field. 4+ years of direct Clinical Supply Chain experience globally. Knowledge of GMP/GxP/GCP and global regulatory requirements (FDA, EU, etc.). Strong clinical supply chain knowledge (packaging, labeling, inventory, global distribution) for accurate forecasting. Understanding of clinical trial operations and the drug development lifecycle. Strong analytical/problem‑solving skills; ability to track forecast accuracy and inventory performance. Excellent communication and stakeholder management to present forecasts, risks, and trade‑offs. Proven ability to operate in a fast‑paced, matrixed environment managing multiple studies. Proficient in MS Office (Excel, PowerPoint, Visio, Project, etc.). #J-18808-Ljbffr