Jobs at Bristol Myers Squibb

Leads clinical supply chain and planning for domestic and international clinical trial product fulfillment. Oversees labeling, packaging, distribution, procurement, vendor and depot relationships, inventory, warehousing, compliance, risk management, and cost optimization. Establishes clinical supply chain teams and processes while partnering with manufacturing, quality, regulatory, finance, and commercial stakeholders. Manages team development, succession planning, and adherence to cGMP, GDP, FDA, and DOT requirements.

Supports clinical trial operations by managing study vendors, CRO activities, budgets, documentation, timelines, risk mitigation, and performance metrics. Assists with protocol and study document reviews, country and site start-up, site feasibility, issue resolution, and Trial Master File quality. The role requires compliance with SOPs, FDA regulations, ICH/GCP guidelines, and study timelines. Up to 10% travel is required.

Manages clinical study vendors and supports CRO, site, and study execution activities in compliance with SOPs, FDA regulations, and ICH/GCP guidelines. Responsibilities include vendor planning, performance tracking, risk mitigation, budgets, invoicing, study start-up, site feasibility, documentation, TMF quality, and escalation of operational issues. The role requires cross-functional collaboration and up to 10% travel.

Lead biostatistician for oncology clinical trials: design statistical strategies, author SAPs and TLFs, validate vendor deliverables, collaborate cross-functionally, support regulatory submissions, pilot AI initiatives, and provide strategic statistical guidance throughout drug development. Travel ~10%.

Lead design, prototyping, and scaling of LLM-enabled AI capabilities for drug discovery research. Partner with scientists and engineers to build agentic systems, evaluation frameworks, grounding and provenance infrastructure, and reusable AI building blocks that improve research decision-making and scientific quality.