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us: Manager, Statistical Programming

             
Apr
16
Bristol-Myers Squibb Company; Princeton, New Jersey, United States
Provides comprehensive programming leadership and support to clinical project teams and vendors, including deployment of programming strategies, standards, specifications and programmed analysis to comply with regulatory requirements, SOPs and work practices; Independently develops, validates, troub...      Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required; At least 7 years programming experience in industry including support of significant regulatory filings; For US positions: US military experience will be considered towards industry experience...

us: Associate Director Biostatistics

             
Apr
09
Bristol-Myers Squibb Company; Princeton, New Jersey, United States
The Associate Director of Biostatistics is a member of cross-functional development teams supporting neuroscience therapeutic area, and contributes to trial design, protocol development, analysis, planning, interpretation of results, and preparation of regulatory submissions. With appropriate experi...      PhD in Biostatistics

us: Associate Director, Biostatistics

             
Mar
29
Bristol-Myers Squibb Company; United States
Collaborates in design of innovative and efficient clinical trials, including the selection of study population/endpoints to address study objectives, and contributes to project development strategy; Defends protocols and analysis plans at internal governance reviews and provides independent reviews...      PhD (6+ years’ experience) or MS (8+ years’ experience) in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experience; Proficiency in scientific computing/programming (SAS, R or Python) and implementation of ad...

us: Director, Biostatistics

             
Mar
28
Bristol-Myers Squibb Company; Princeton, New Jersey, United States
Drives innovative and efficient study design. Develops study designs that address study objectives that will support regulatory approval, medical research and market access; Independently leads, initiates, and oversees the statistical support for the development of compounds within a therapeutic are...      PhD (9+ years experience) or MS (11+ years experience) in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experience; Proficiency in scientific computing/programming (SAS, R or Python) and implementation of advance...

us: Associate Director, Biostatistics

             
Mar
28
Bristol-Myers Squibb Company; United States
Collaborates in design of innovative and efficient clinical trials, including the selection of study population/endpoints to address study objectives, and contributes to project development strategy; Defends protocols and analysis plans at internal governance reviews and provides independent reviews...      PhD (6+ years’ experience) or MS (8+ years’ experience) in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experience; Proficiency in scientific computing/programming (SAS, R or Python) and implementation of ad...
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