Global Trial Supply Strategy Lead

Bristol Myers Squibb; Dublin; Hybrid; EUR 120,000 - 160,000; Full time

Job summary

Bristol Myers Squibb is seeking a Senior Manager, Trial Supply Management to lead senior-level accountability for supply strategies of investigational products within a global clinical framework. The role emphasizes collaboration across GCSC, PDQ, external vendors, and cross-functional teams to ensure timely delivery within regulatory constraints.

Based in a global, patient-centric environment, this position requires strategic planning, robust leadership, and strong negotiation skills to

Qualifications

• Minimum 5+ years Pharma industry related experience.
• Minimum 3 years Clinical Supplies / Development with global experience or equivalent experience.
• Advanced knowledge of the global drug development process and global regulatory requirements.
• Advanced analytical skills.
• Advanced communication and negotiation skills.
• Advanced project management skills.
• Strong knowledge of import/export requirements.
• Strong knowledge of IVRS and CTMS systems.

Responsibilities

• Collaborates with internal GCSC teams and external Customers and Service Providers to meet needs.
• Plans and communicates the clinical supply chain strategy for global studies.
• Drives continuous improvement to supply strategies for investigational products.
• Interacts with CSL to align study timelines and protocol amendments.
• Monitors inventory and analyzes drug utilization vs. forecast across countries and timelines.
• Authors and reviews Change Controls and eTMF related documents.
• Supports distribution strategies and IRT specifications as required.
• Leads internal Clinical Supply Chain meetings and risk mitigation discussions.

Skills

Pharma industry experience

Clinical supplies

Communication skills

Negotiation

Project management

Regulatory knowledge

Supply chain planning

Leadership

Job description

Bristol Myers Squibb is seeking a Senior Manager, Trial Supply Management to lead senior-level accountability for supply strategies of investigational products within a global clinical framework. The role emphasizes collaboration across GCSC, PDQ, external vendors, and cross-functional teams to ensure timely delivery within regulatory constraints.

Based in a global, patient-centric environment, this position requires strategic planning, robust leadership, and strong negotiation skills to