Jobs 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.

Provides medical accountability and oversight for Phase 2-3 clinical trials, including medical monitoring, safety assessment, protocol input, investigator engagement, and regulatory document authorship. Leads cross-functional teams, supports study execution, and represents medical expertise in health authority interactions and publications.

Lead agile, project-based design and delivery of global commercialization learning programs. Conduct needs assessments, design scalable skills-based pathways, partner with LEAP and vendors, integrate platforms and AI tools, track learner analytics, and drive stakeholder governance, localization, and continuous improvement across Commercial, Medical, Market Access, and Field teams.

Lead translation of national market access strategy into regional execution across the UK and Ireland. Build a Centre of Excellence, design and deliver training, create market access tools (dossiers, payer decks, budget impact models), generate data-driven regional insights, partner with IHMs and cross-functional teams, and ensure compliance with ABPI and internal governance to improve formulary access and reduce time-to-access.

Lead development and implementation of novel statistical methods and study designs for drug development. Provide statistical consulting, drive stakeholder engagement, oversee tools/software development, publish and present research, and mentor junior methodologists while collaborating across cross-functional teams.

Lead biostatistical contributions across clinical development: design trials, draft SAPs/protocols, analyze and interpret results, support regulatory submissions, and collaborate with cross-functional teams to ensure quality and alignment.

Lead quality and compliance efforts for global clinical trials, executing risk management programs, and fostering a culture of quality excellence. Responsible for identifying business risks and managing cross-functional teams.

Lead statistical programming for clinical trials: produce submission-ready outputs using SAS and CDISC standards, implement ADaM specs and e-submission components, review SAPs, advise stakeholders, mentor/coach programmers, and drive process improvements across cross-functional teams.