Jobs at Bristol Myers Squibb

Lead biostatistics activities on clinical development teams: design studies, author/review protocols and SAPs, perform/validate analyses, interpret and communicate results, ensure SOP compliance, mentor staff, and support regulatory submissions.

Lead global and US regulatory strategy for development programs, create submission plans, engage health authorities, oversee regulatory documents and dossiers, manage external vendors and cross-functional teams, and resolve critical regulatory issues to enable product registration.

Lead architecture and engineering of enterprise AWS cloud platform and CI/CD pipelines. Build and maintain IaC (CloudFormation), enforce SecDevOps and governance, integrate AI/ML into SDLC, optimize costs, and mentor teams while delivering scalable, production-ready cloud solutions.

As a Senior Data Scientist, you will lead AI product hypotheses and experimentation, working with cross-functional teams to develop and evaluate AI solutions across various company functions. Responsibilities include designing datasets, building analytical features, and measuring product impacts using AWS tools and industry-best practices.

Provide scientific and technical leadership for data science across drug development programs. Design and execute analyses on multimodal clinical and omics data, develop predictive models and AI/ML methods, define reproducible pipelines (Python/R/SQL/cloud), mentor data scientists, influence trial and biomarker strategy, and translate results to inform clinical development decisions.

Lead strategy and delivery of clinical pharmacology and pharmacometrics technology, modeling environments, and automated workflows. Partner with R&D, data, labs and regulatory teams to ensure scalable, auditable, inspection-ready CPP systems, reporting, and model-informed decision support. Build and grow a specialized scientific technology team and drive automation, AI-enabled analytics, and regulatory submission support.

Design, implement, and deploy end-to-end machine learning pipelines to optimize clinical trial operations. Collaborate with cross-functional teams to integrate AI solutions, manage AI product lifecycles, monitor post-deployment performance, and translate model outputs into actionable clinical operations strategies. Stay current on AI trends including NLP and predictive analytics.

Provide medical accountability and oversight for multiple early-phase oncology clinical trials (Phase I/II), serving as Medical Monitor, designing clinical strategy, liaising with cross-functional teams, contributing to regulatory submissions, assessing safety events, establishing Phase I center relationships, and representing the program externally.

Lead global regulatory strategy for Neuroscience development and marketed products. Serve as primary interface with health authorities, build global regulatory plans, advise cross-functional teams, evaluate regulatory landscape, support due diligence and submissions, and guide regional regulatory staff to align development and commercialization strategies.

The Senior Application Engineer will develop cloud-native applications and APIs, focusing on AI products, utilizing AWS technologies, and engaging in Agile project cycles.

Lead and develop a therapeutic-area team of scientific writers, applying advanced regulatory documentation expertise to create content libraries, standardize processes and tools, and drive document automation initiatives. Provide managerial, scientific, and customer-focused leadership to ensure consistent regulatory documentation across development and lifecycle management globally.

Lead and execute biomarker and drug development data science efforts: develop computational methods and predictive models for multimodal clinical and omics data, perform high-dimensional statistical analyses, partner with statisticians and translational scientists on protocols and SAPs, validate biomarker assays for trials, implement scalable ML/DL solutions, and manage cross-functional resources to deliver quality results on timelines.

Provide medical accountability and oversight for Phase 1–3 immunology clinical trials, leading medical monitoring, protocol design, safety assessments, regulatory writing, investigator engagement, and cross-functional study delivery while ensuring GCP compliance and contributing to clinical strategy and scientific leadership.

Bench-facing translational research role supporting preclinical and early clinical oncology studies. Design and execute in‑vitro and ex‑vivo assays, validate clinical-stage assays, analyze genomic/proteomic data, collaborate across cross-functional teams, and translate clinical observations into preclinical experiments to support biomarker and therapeutic development.

The Director of Biostatistics leads innovative clinical trial designs, manages statistical resources, ensures compliance with standards, and develops strategies for regulatory submissions. The role also involves mentoring team members and representing the company in professional settings.

The Senior Director leads the Biostatistics function, guiding statistical contributions in clinical development, managing budgets, ensuring compliance, and mentoring the team, while collaborating with regulatory agencies and driving strategy improvement.

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 global diagnostic and companion imaging radiopharmaceutical development (PET/SPECT) from candidate nomination through CMC, tech transfer, regulatory submissions, manufacturing scale-up, lifecycle management, and health authority interactions. Build and manage cross-functional teams, ensure compliance with radiopharmaceutical regulations, coordinate global regulatory strategy, manage external CDMO/CRO partners, and align imaging programs to support patient selection, dosimetry, and RLT clinical objectives.

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%.