Senior Manager, Trial Supplies Management

Bristol Myers Squibb

Senior Manager responsible for supply strategies for investigational products at Bristol Myers Squibb. Collaborating with global teams and ensuring compliance with drug development regulations.

Posted 7/14/2026full-timePrinceton • New Jersey • 🇺🇸 United StatesSenior💰 $134,170 - $162,586 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates advanced knowledge of the global drug development process, regulatory requirements, and clinical supply chain strategies. Proficient in project management, analytical skills, and effective communication to enhance the delivery of clinical supplies.

Highest-signal resume keywords

Clinical Supply Chain StrategyGlobal Drug Development ProcessAdvanced Project ManagementAnalytical SkillsIVRS and CTMS Systems

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Supplies ManagementRegulatory RequirementsProject ManagementAnalytical SkillsSupply Chain StrategyPackaging and LabelingLogisticsQuality AssuranceImport/Export RequirementsContinuous Improvement Strategies

Soft Skills

Communication SkillsNegotiation SkillsCollaborationConflict Management

Tools & Technologies

IVRSCTMSInteractive Response Technology

Industry Keywords

Pharma IndustryClinical DevelopmentInvestigational ProductsGlobal ExperienceSupply Chain Operations

About the role

Key responsibilities & impact

Collaborates with internal Global Clinical Supply Chain (GCSC) teams and external Customers and Service Providers.
Partners with the Clinical Supply Lead (CSL) in planning and communicating the clinical supply chain strategy.
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.
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.
Monitors inventory and analyzes drug utilization versus forecast based on country requirements and logistical timelines.
Issues Packaging/Labeling requests to Clinical Supply Operations (CSO).
Support use date extension activities, such as generation of Use Date Extension (UDE) memo.
Derives enhancements to improve the timely delivery of quality clinical supplies for all assigned compounds and protocols by collaborating with internal and external sources.
Participates in development, review and approval of Interactive Response Technology (IRT) specifications.
Executes investigational product distribution strategies and maintains distribution and supply strategies at depot and site level.
Actively participates in internal Clinical Supply Chain meetings and provides relevant data and documentation prior to each meeting.
Collaborates with Clinical Supply Strategic Sourcing team to procure commercial drug in alignment with country and clinical study requirements.
Manages conflicts/issues with internal and external partners and customers.

Requirements

What you’ll need

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.
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.

Benefits

Comp & perks

Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work-life benefits include: Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays).
Based on eligibility, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.