Jobs at Bristol Myers Squibb

Lead development and application of computational and statistical methods for biomarker discovery and patient segmentation using multimodal clinical, omics, and real-world data. Partner with statisticians and scientists to write and defend analysis plans, build predictive ML/DL models, coordinate biomarker analyses for trials and RWD, validate assays, mentor team members, and communicate results to support drug development and regulatory submissions.

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.

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.

Design and maintain reusable GenAI architectures, templates, and components; enable and embed with AI Accelerator pods to solve complex technical problems; provide technical leadership, mentorship, and promote responsible AI practices for scalable enterprise adoption.

Design, build, and operate secure AWS-native backend services, APIs, and agent runtimes for agentic AI products. Implement retrieval, semantic layers, CI/CD, observability, sandboxed execution, and infrastructure-as-code while partnering across cross-functional pods to deliver and scale MVPs.

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 Senior Director of Translational Research will lead strategic initiatives in protein homeostasis, integrating preclinical biology with clinical strategies, and overseeing team development within a collaborative environment.

The Senior Director of Clinical Pharmacology & Pharmacometrics will lead CPP technology and workflow improvements, ensuring operational excellence and supporting regulatory submissions in pharmaceutical development.

Lead strategic drug development and commercialization for oncology targeted therapies, ensuring high-quality asset delivery through cross-functional team collaboration and regulatory compliance.

The Radiopharmaceutical Applications Liaison supports clinical adoption of radiopharmaceutical products, educates stakeholders, and ensures compliance with regulations, while generating actionable insights for strategy development.

Coordinate, curate, validate, and maintain high-quality, reproducible research datasets for translational and clinical studies. Manage vendor/CRO data transfers, perform QC and data queries, develop data management plans and AI-ready datasets, collaborate with scientists and data engineers, and support data governance, standardization, and tooling to enable analytics and digital transformation across R&D.

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.