Description

You will manage end-to-end clinical supply chain for multiple programs, ensuring timely delivery of investigational products in compliance with regulations. Collaborate cross-functionally to develop supply strategies and optimize operations.

Requirements

• Highly motivated and results-oriented
• Experience in clinical supply chain management
• Knowledge of GMP and regulatory guidelines (FDA, EMA, ICH)
• Ability to manage vendor relationships
• Experience with IRT systems and UAT

Responsibilities

• Develop and implement clinical supply strategies to meet study timelines
• Prepare demand forecasts using simulation tools
• Partner with stakeholders to determine demand assumptions
• Optimize supply chain operations to minimize waste
• Oversee procurement, packaging, labeling, distribution, and return of clinical trial materials