Description

You will oversee global clinical supply chain activities for late-stage trials, including procurement, labeling, distribution, and inventory management. You'll collaborate cross-functionally to ensure timely, compliant delivery of investigational products. Drive strategic planning and process improvements to support breakthrough gene therapies.

Requirements

• Bachelor's degree in supply chain or other disciplines with equivalent industry experience.
• 8+ years of experience in clinical or commercial supply chain management, with at least 3 years in a senior or managerial role.
• In-depth knowledge of clinical trial processes, GMP, GCP, and regulatory requirements.
• Proven experience managing complex global supply chains for clinical trials (including Europe, APAC, and South America).
• Proven experience with high-complexity Phase 3 trials.
• Strong project management skills.
• Excellent negotiation, communication, and interpersonal skills.
• Proficiency in supply chain management software and tools.
• Strong analytical and problem-solving abilities.
• Ability to work in a fast-paced, dynamic environment.

Responsibilities

• Develop and implement clinical supply strategies to support global clinical trials.
• Lead Phase 1 to 3 clinical trial materials planning and execution.
• Oversee material requirements for domestic and international study execution.
• Manage inventory levels to ensure sufficient supply while minimizing waste.
• Coordinate distribution of clinical supplies to CMOs and study sites.
• Identify, select, and manage relationships with suppliers, manufacturers, and logistics providers.
• Negotiate contracts and service agreements with vendors.
• Generate and maintain clinical supply inventory reports.
• Drive continuous operational performance improvement efforts.
• Ensure compliance with GMP and regulatory requirements.