Associate Director, Biostatistics | United States | Bristol-Myers Squibb Company

Position:	Associate Director, Biostatistics
Institution:	Bristol-Myers Squibb Company
Location:	United States
Duties:	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 of complex protocols; Independently authors and/or reviews protocol, statistical analysis plan, clinical study reports, associated publications, and other study level documents; Presents summary data and analyses results, in a clear, concise, complete, and transparent manner; Provides statistical support and leadership to address health authority request, publication, presentation, and other public release of information
Requirements:	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 advanced statistical analysis, data manipulation, graphing & simulation; Great interpersonal, communication, writing and organizational skills; Expertise in statistical/clinical trials methodology as it related to clinical development and ability to apply to relevant clinical development framework

Text:	Associate Director, Biostatistics 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 of complex protocols; Independently authors and/or reviews protocol, statistical analysis plan, clinical study reports, associated publications, and other study level documents; Presents summary data and analyses results, in a clear, concise, complete, and transparent manner; Provides statistical support and leadership to address health authority request, publication, presentation, and other public release of information 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 advanced statistical analysis, data manipulation, graphing & simulation; Great interpersonal, communication, writing and organizational skills; Expertise in statistical/clinical trials methodology as it related to clinical development and ability to apply to relevant clinical development framework