Jobs at Bristol Myers Squibb

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 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.

Develop and validate SAS programs to produce derived analysis datasets and TFLs, prepare e-submission packages (NDA/BLA/MAA), review SAPs and data presentation plans, partner with vendors on standards and file transfers, independently lead programming assignments across multiple projects, and contribute efficiency and consistency improvements across the Global Biometrics & Data Sciences function.

The Senior Manager, Data Sciences role focuses on developing novel computational methods and predictive models from complex clinical data to drive drug development insights.

The Senior Manager, Biostatistics contributes to trial design and analysis planning, communicates with clinical partners, and prepares regulatory submissions, ensuring quality in statistical deliverables.

Lead data science strategy and hands-on advanced analytics for drug development programs. Design and execute multimodal analyses (omics, imaging, EHR), develop AI/ML and statistical models, ensure reproducible pipelines, mentor a small team, and partner cross-functionally to influence trial design, biomarker strategy, and regulatory decision-making.

Lead end-to-end clinical data management for complex trials, set data collection strategy, own the data lifecycle, define EDC requirements, chair data quality reviews, author key study documents, mentor junior leads, oversee vendors/CROs, support regulatory submissions and audits, and drive continuous improvement in clinical data processes.

Lead end-to-end clinical data management for complex programmes: set programme-level standards, oversee EDC and integrations (eCOA, external data, Safety Gateway), manage vendors/CROs, author study documentation, support inspections/audits, mentor leads, and represent data management cross-functionally.

Provide medical leadership and oversight for Phase 1-3 clinical trials, leading medical monitoring, safety evaluations, protocol development, and GCP compliance. Partner with clinical development teams on study design, benefit/risk analyses, site interactions, and regulatory submissions. Build KOL relationships and represent the company at health authority and advisory meetings; travel domestically and internationally as required.