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The Senior Manager of Statistical Programming leads statistical programming teams to support the development and regulatory approval of products at Bristol Myers Squibb. Responsibilities include designing and implementing technical solutions for clinical data analysis and reporting, managing teams, and leading improvement initiatives for programming processes.

The Senior Manager of Biostatistics collaborates on trial design, analysis planning, and regulatory submissions, guiding teams in statistical analysis and methodology compliance while enhancing their knowledge of drug development.

The Associate Director will develop innovative statistical methods, provide consulting for projects, and mentor junior staff while collaborating across teams in biostatistics and data science.

The Associate Director, Biostatistics leads statistical aspects for clinical trials, including study design, result presentation, and regulatory submissions. They collaborate with cross-functional teams and ensure quality in project execution.

The Associate Director of Biostatistics leads statistical input for clinical trials, manages study designs and analysis plans, and ensures regulatory compliance.