The selected candidate will be responsible for study supply leadership to ensure timely planning and execution of supply strategy for continued supply of clinical finished goods (supply drugs) to patients.
Furthermore, he will be in charge for optimal clinical trial supply strategy in terms of packaging design, pro-active planning following a risk-based approach. In this role the successful candidate reports to Head of CMC, located in the US.


Your responsibilities include: 

• Supply Chain Management: Develop and implement clinical supply chain strategies, including packaging, labeling, distribution, and return or destruction of clinical supplies.
• Collaboration: Work closely with clinical operations, project management, and manufacturing teams to establish clinical supply plans.
• Forecasting: Predict the need for clinical supplies and ensure timely and cost-effective delivery.
• Inventory Management: Monitor and manage inventory levels to prevent stockouts or overstocking.
• Compliance: Ensure compliance with regulatory guidelines and Good Manufacturing Practice (GMP) standards.
• Vendor Management: Participate in the selection of vendors and the negotiation of contracts.
• Documentation: Review and approve clinical supply documents such as packaging instructions and shipping documents.
• Risk Management: Implement strategies to mitigate supply chain disruption