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Senior Manager RWE Biostats

Bristol Myers Squibb
September 22, 2026
Full-time
Remote friendly (Princeton, NJ)
Worldwide
Clinical Research and Development
Role: Senior Manager of RWE Biostatistics, contributing to real-world evidence (RWE) study design, analysis, interpretation, and regulatory documentation within biopharma. Responsibilities: collaborate on methodology development, author/review statistical analysis plans, perform analyses, communicate findings to cross-functional teams, ensure compliance with global standards, and enhance technical expertise in RWE methodologies. Qualifications: PhD or MS with 2+ years in biostatistics/statistics, experience with clinical trial or RWE data, proficiency in SAS, R, or Python, and strong communication skills. Preferred: knowledge of advanced statistical methods, regulatory requirements, and experience in drug development processes. High-Value: focus on RWE studies, data analysis for regulatory submissions, and cross-functional collaboration. Work setup: location details not specified, with emphasis on collaborative environment.