Jobs at Bristol Myers Squibb

Manage radiopharmaceutical therapy patient dose scheduling and clinical material delivery across clinical programs. Responsibilities include tracking study and site dosing schedules, coordinating clinical, supply chain, logistics, radiochemistry, and manufacturing stakeholders, processing drug product orders, mitigating delivery risks, maintaining site procedures, and implementing continuous planning and scheduling improvements. The role also supports scheduling simulations, operational continuity, regulatory compliance, and approximately 10% travel.

Manages clinical study vendors and supports CRO, site, and study execution activities for biotech clinical trials. Responsibilities include vendor planning, performance tracking, risk mitigation, budgets, invoicing, study start-up, site feasibility, documentation, TMF quality, and issue escalation. Ensures compliance with SOPs, FDA regulations, and ICH/GCP guidelines while supporting study timelines, budgets, and quality. The role requires up to 10% travel and collaboration across cross-functional teams.

Lead planning, execution, and reporting of supplier and service provider audits to ensure cGMP/GxP compliance. Evaluate regulatory adherence, document observations, drive CAPAs to closure, support inspection readiness, provide training, and participate in continuous improvement. Domestic travel ~10-15%.

Lead and execute non-interventional retrospective oncology research using large datasets; develop protocols, perform statistical programming and analyses, communicate results to stakeholders, provide methodological leadership, mentor staff, and collaborate with HEOR, medical, and market access teams to support value-focused outcomes research.

Lead and execute clinical data management strategy across oncology studies, ensuring database build, validation, cleaning, and lock for NDA submissions. Manage and grow the data management team, oversee CROs and vendors, implement SOPs and automation, ensure inspection readiness, and partner cross-functionally to maintain high-quality, compliant data deliverables.

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.