Sr. Manager

Role: Senior Manager of Biostatistics, contributing to clinical trial design, protocol development, analysis, and regulatory submission within biopharma drug development. Responsibilities: collaborate on study methodology, author/review key statistical documents, perform/validate analyses, interpret results, and communicate findings to cross-functional teams. Ensure compliance with BMS standards and continuously develop expertise in statistical methods, regulatory requirements, and drug development processes. Qualifications: PhD (3+ years) or MS (5+ years) in statistics, biostatistics, or related field; proficiency in SAS, R, or Python; strong communication and organizational skills; experience with clinical trials, regulatory guidelines, and advanced statistical techniques preferred. High-Value Details: Focus on biopharma clinical development, with emphasis on therapeutic areas relevant to BMS's pipeline; role involves cross-functional collaboration, regulatory compliance, and quality standards; work may be hybrid or onsite depending on role design, with some travel requirements.