Teams at Bristol Myers Squibb

Provide medical accountability and oversight for Phase 1-3 immunology clinical trials. Lead medical monitoring and safety assessments, contribute to protocol design and clinical strategy, support study execution and site interactions, engage key opinion leaders and health authorities, and author clinical/regulatory documents in partnership with cross-functional teams.

Develop and validate SAS programs to create derived analysis datasets and TFLs; prepare electronic submission packages; review SAPs and data presentation plans; partner with vendors and cross-functional teams; independently lead programming assignments and drive GBDS efficiency improvements.

Lead SDTM strategies and technical programming for clinical studies from protocol review through global regulatory submission. Own SDTM mapping, metadata-driven automation, Pinnacle 21 validation, eCRT packages, cross-functional data integration, CRO/vendor oversight, and mentor junior programmers to ensure high-quality, submission-ready deliverables.