Senior Trial Supply Strategy Leader

Bristol Myers Squibb UK & Ireland; Dublin; Hybrid; EUR 120,000 - 150,000; Full time

Benefits offered by this job

Competitive salary

Benefits package

Inclusive culture

Job summary

Bristol Myers Squibb in Ireland seeks a Senior Manager, Trial Supply Management to provide senior-level accountability for supply strategies of investigational products across global studies, ensuring alignment with regulatory constraints.

You will collaborate with GCSC, CSL, external partners, and internal teams to optimize clinical supply chains, drive continuous improvement, manage risk, and support protocol amendments and distribution strategies across depots and sites.

Qualifications

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

Responsibilities

• Collaborates with internal Global Clinical Supply Chain (GCSC) teams and external Customers and Service Providers to ensure all needs are met.
• Partners with the Clinical Supply Lead in planning and communicating the clinical supply chain strategy for global studies.
• Formulates and drives continuous improvement of supply strategies for investigational products.
• Monitors study timelines, protocol amendments, and distribution strategies across depots and sites.
• Ensures regulatory compliance and leads risk mitigation in supply activities.
• Writes and maintains departmental procedural documents and supports inspection readiness.

Skills

Pharma industry experience

Clinical supplies

Global experience

Regulatory knowledge

Analytical skills

Communication skills

Project management

Leadership

Negotiation

Cross-functional collaboration

Tools

IVRS

CTMS

Job description

Bristol Myers Squibb in Ireland seeks a Senior Manager, Trial Supply Management to provide senior-level accountability for supply strategies of investigational products across global studies, ensuring alignment with regulatory constraints.

You will collaborate with GCSC, CSL, external partners, and internal teams to optimize clinical supply chains, drive continuous improvement, manage risk, and support protocol amendments and distribution strategies across depots and sites.