Senior Trial Supply Lead, Global Clinical Ops

Bristol-Myers Squibb; Dublin; On-site; EUR 120,000 - 150,000; Full time

Job summary

Bristol Myers Squibb is seeking a Senior Manager, Trial Supply Management to lead supply strategies for investigational products across global studies. You will oversee planning, execution, and continuous improvement with internal and external partners.

The role requires senior-level accountability and collaboration across Clinical Supply Chain functions to ensure timely and compliant distribution of clinical materials. A pro-active leader with deep regulatory knowledge will thrive.

Qualifications

• Minimum 5+ years Pharma industry related experience.
• Minimum 3 years Clinical Supplies / Development with global experience or equivalent experience.
• 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 proficient knowledge of related areas i.e., Manufacturing, Packaging & Labeling, IVRS, Logistics, Quality, Stability, etc.
• Strong knowledge of import / export requirements.
• Strong knowledge of IVRS and CTMS systems.
• Advanced knowledge of industry technology and how to apply source innovative solutions and new industry best practices.
• Develops and applies unique ideas and new methods to achieve higher performance and excellence.
• Team and individual leadership (leads courageously).
• Oral and written communication (fosters open communication).
• Conflict resolution (manages disagreements).
• Negotiation (Manages Execution, Results Driven, Analysis of Issues, Effective Speaking, Builds Relationships).
• Influencing (manages influencing others).
• Delegating (provides direction).
• Coaching and mentoring (fosters teamwork).

Responsibilities

• Collaborates with internal Global Clinical Supply Chain (GCSC) teams and external Customers and Service Providers, including but not limited to Global Drug Development, Pharmaceutical Development, Product Development Quality (PDQ), External Vendors and Medical to ensure all needs are met.
• Partners with the Clinical Supply Lead (CSL) in planning and communicating the clinical supply chain strategy in support of global clinical studies to ensure optimal use and alignment with study and corporate goals.
• Demonstrates robust knowledge and confidence of GCSC processes when presenting at cross-functional meetings.
• Formulates and drives strategies for continuous improvement to supply strategies for investigational products, both departmental and/or inter-departmental.
• Influences clinical and development timelines, study design and country selection.
• Responsible for reviewing and working with the CSL to provide any contributions to the clinical protocol and directly responsible for protocol amendments, communicating timelines and investigational product strategies to study and cross-functional teams.

Skills

Pharma experience

Clinical supplies

Education substitution

Drug development process

Analytical skills

Communication

Project management

Planning

Import/Export knowledge

IVRS/CTMS

Innovation/Tech

Leadership

Oral/Written communication

Conflict resolution

Negotiation

Influencing

Delegation

Coaching

Job description

Bristol Myers Squibb is seeking a Senior Manager, Trial Supply Management to lead supply strategies for investigational products across global studies. You will oversee planning, execution, and continuous improvement with internal and external partners.

The role requires senior-level accountability and collaboration across Clinical Supply Chain functions to ensure timely and compliant distribution of clinical materials. A pro-active leader with deep regulatory knowledge will thrive.