Associate Director, Clinical Supply Chain
Core
Leads end-to-end clinical supply chain activities for a global clinical-stage portfolio, translating study assumptions into demand forecasts, supply plans, and execution strategies to ensure investigational product availability.
Role type
Associate Director, Clinical Supply Chain
Builds
Investigational product supply from production/release through packaging, distribution, and trial completion
Domain
Biopharmaceuticals / Clinical Trials / Supply Chain
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical supply chain management, Drug forecast planning, GxP compliance (cGMP, GCP, 21 CFR Part 11, Annex 13), Budget management, Vendor management, Risk mitigation, Project planning, Stakeholder collaboration
Preferred skills
Manufacturing experience, Quality function exposure, Regulatory function exposure, Secondary packaging/labeling expertise, RTSM system knowledge
Technologies
Microsoft Excel, Microsoft PowerPoint, Microsoft Project, Office Timeline
Responsibilities
Translate clinical trial assumptions into drug forecasts and distribution strategies; Lead end-to-end clinical supply execution; Serve as liaison with Clinical Operations, CMC, Quality, and Regulatory teams; Manage clinical supply budgets and vendor invoices; Oversee secondary packaging, labeling, and final drug release; Mitigate end-to-end supply chain risks; Ensure compliant documentation for Trial Master Files and Clinical Study Reports.
Seniority
Senior, hands-on IC with strategic leadership