Clinical Supply Manager

On behalf of a leading global pharmaceutical company, we are seeking a highly motivated and detail-oriented Clinical Supply Manager to join an international and innovative organization dedicated to developing advanced pharmaceutical products for oncology and diagnostic imaging.

This position offers the opportunity to take responsibility in complex end-to-end clinical supply chains supporting global clinical studies. The successful candidate will be responsible for establishing, planning, coordinating, and executing clinical supply activities to ensure investigational medicinal products (IMPs) and imaging products are available at clinical sites in the right quantity, at the right time, and in full compliance with applicable to quality and regulatory requirements. Furthermore, perform supply performance, inventory levels of a commercial product based on demand forecasts.

Key Responsibilities

• Develop and maintain clinical supply strategies and plans aligned with clinical study protocols and enrollment forecasts.
• Manage ordering, manufacturing coordination, materials, packaging, labeling, distribution, and inventory management of IMPs and imaging products.
• Establish and implement clinical supply operations for new countries, depots, and clinical study sites.
• Coordinate activities with Clinical Operations, Quality Assurance, Regulatory Affairs, CMC, external depots, and Contract Manufacturing Organizations (CMOs).
• Provide oversight and support for supply and material-related activities connected to commercial product.
• Monitor supply performance, inventory levels, demand forecasts, and key performance indicators.
• Identify supply chain risks and implement mitigation plans to ensure uninterrupted supply.
• Drive continuous improvement initiatives across clinical supply processes and systems by implementing IRT systems, AI tools and digital solutions.
• Ensure compliance with GMP, GDP, GCP, and applicable regulatory requirements.
• Maintain compliant supply documentation, procedures, and quality records.
• Support deviations, investigations, and change control activities.