Senior Global Clinical Trial Supply Manager

Bristol Myers Squibb EU Policy; Dublin; On-site; EUR 120,000 - 170,000; Full time

Benefits offered by this job

Competitive salary

Great benefits package

Job summary

Bristol Myers Squibb is seeking a Senior Manager, Trial Supply Management to lead senior-level accountability for investigational product supply strategies within a global clinical setting.

The role involves coordinating with internal GCSC teams and external partners to ensure timely, compliant delivery of clinical supplies, monitoring inventory, and shaping strategic supply chain decisions across global studies.

Qualifications

• Minimum 5+ years Pharma industry related experience.
• Minimum 3 years Clinical Supplies / Development with global experience or equivalent.
• An equivalent combination of education and experience may substitute.
• Advanced knowledge of the global drug development process and global regulatory requirements.
• Advanced analytical skills.
• Advanced communication and negotiation skills.
• Advanced project management skills.
• Advanced knowledge of planning and related areas (Manufacturing, Packaging & Labeling, IVRS, Logistics, Quality, Stability).
• Strong knowledge of import / export requirements.
• Strong knowledge of IVRS and CTMS systems.
• Advanced knowledge of industry technology and applying innovative solutions.

Responsibilities

• Collaborates with internal GCSC teams and external Partners to ensure all needs are met.
• Planning and communicating the clinical supply chain strategy in support of global clinical studies.
• Formulates and drives strategies for continuous improvement to supply strategies for investigational products.
• Influences timelines, study design and country selection; contributes to clinical protocol and amendments.
• Monitors inventory and analyzes drug utilization versus forecast.
• Issues packaging/labeling requests to CSO to ensure regulatory compliance.
• Supports use date extension activities and labeling.
• Develops and applies ideas to improve timely delivery of clinical supplies.
• Participates in development, review and approval of IRT specifications and distribution strategies.
• Participates in internal meetings and highlights risks and mitigations.
• Collaborates with Compliance to prepare eTMF, CSR appendices and batch listings.
• Manages conflicts with partners and customers.
• Writes departmental procedural documents.

Skills

Pharma experience

Clinical supplies

Global regulatory knowledge

Job description

Bristol Myers Squibb is seeking a Senior Manager, Trial Supply Management to lead senior-level accountability for investigational product supply strategies within a global clinical setting.

The role involves coordinating with internal GCSC teams and external partners to ensure timely, compliant delivery of clinical supplies, monitoring inventory, and shaping strategic supply chain decisions across global studies.