Senior Trial Supplies Manager
Bristol Myers Squibb (company site, opens in a new tab)5+ yrsHyderabadOn-siteDirect career pageEst. 18–28 LPA
Posted 8h ago
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Job description
Structured overview of role & requirements
About This Role
- Develop and maintain supply strategies for investigational products across global clinical studies ensuring alignment with development plans and regulatory requirements.
- Collaborate with cross-functional internal teams and external vendors to ensure timely delivery of clinical supplies, including forecasting, inventory monitoring, and distribution strategy.
- Lead communications and act as main contact for clinical supply strategy, contribute to protocol reviews, budget processes, and risk mitigation throughout clinical trials.
Minimum Requirements
- Minimum 5+ years pharmaceutical industry experience.
- At least 3 years in Clinical Supplies/Development with global experience or equivalent.
- Advanced knowledge of global drug development processes, global regulatory requirements, and supply chain functions including Manufacturing, Packaging & Labeling, IVRS, and Logistics.
- Strong knowledge of import/export requirements and clinical trial management systems (IVRS, CTMS).
Ideal Candidate Profile
- Experienced in managing complex clinical supply chains with demonstrated ability to influence study design, timelines and supply strategies at global level.
- Skilled in project management, forecasting, cross-functional collaboration, and vendor management in pharmaceutical clinical trials.
- Able to mentor others and lead issue resolution ensuring clinical supply alignment with regulatory and quality standards.