Teams 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%.