Clinical Supply Chain Manager
On-site · Zebulon, North Carolina, United States or Siena, Tuscany, Italy
Job Summary
Lead end-to-end clinical supply planning and delivery for assigned investigational assets; collaborate with clinical teams, quality, regulatory and external partners to design patient-focused, risk-adjusted supply strategies; influence clinical decisions, manage risks, and ensure timely delivery of clinical trial materials; oversee packaging, labeling, and distribution activities; manage IRT specifications, testing and maintenance to support randomization and supply control; proactively identify supply risks and lead mitigation activities; track program costs, budgets and supplier contracts; collaborate with cross-functional teams to ensure alignment with project timelines and regulatory requirements.
Required Qualifications
- 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 quality and regulatory expectations (cGMP, GCP, ICH, or equivalent)
- Experience working with cross-functional teams and effectively communicating supply constraints and possible solutions to clinical and project leadership
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