Senior Clinical Supply Chain Planner

The Sr. Clinical Supply Chain Planner will be responsible for overseeing end-to-end clinical supply chain activities for assigned clinical trials. This role will work cross-functionally with Clinical Operations, Global Planning, Quality, Regulatory Affairs, CMOs, and CROs to ensure seamless supply of clinical trial materials. The ideal candidate will be a hands-on professional with experience in supply and demand forecasting, IRT/UAT setup, labeling, packaging, and vendor management.

Requirements

• Manage packaging, labeling, and distribution of clinical trial materials.
• Support IRT (Interactive Response Technology) setup, user acceptance testing (UAT), and system maintenance.
• Develop, monitor, and optimize clinical supply and demand forecasts.
• Create and execute supply strategies to minimize waste and maximize efficiency.
• Oversee label creation and approval, including translation management and compliance with global regulatory requirements.
• Coordinate supply requirements with Global Planning to ensure timely and accurate material availability.
• Manage study and program budgets, monitor KPIs, and identify opportunities for cost savings.
• Build and maintain strong partnerships with third-party vendors (CMOs/CROs) to ensure compliant and efficient operations.
• Maintain accurate documentation, including eTMF filing for clinical supply records.

Benefits

• 6- month contract