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Position: Sr. Manager Biostatistics
Institution: Bristol-Myers Squibb Company
Location: Princeton, New Jersey, United States
Duties: Collaborates in design of clinical study including methodology, data analysis & interpretation, and reporting of study results; Authors and/or reviews protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, associated publications, and other study level specification documents under some supervision; Performs and/or validates statistical analyses, advise ways to maximize clarity of data display; Communicates results to cross-functional teams, provides data interpretation in study documents such as clinical study reports, and publications; Translates scientific questions into statistical terms and statistical concepts into layman terms; Compliant with BMS processes and SOPs, adherence to global and project standards within an indication or therapeutic area and responsible for quality of deliverable
Requirements: Fresh PhD or MS with 2+ 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
   
Text: Sr. Manager Biostatistics Collaborates in design of clinical study including methodology, data analysis & interpretation, and reporting of study results; Authors and/or reviews protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, associated publications, and other study level specification documents under some supervision; Performs and/or validates statistical analyses, advise ways to maximize clarity of data display; Communicates results to cross-functional teams, provides data interpretation in study documents such as clinical study reports, and publications; Translates scientific questions into statistical terms and statistical concepts into layman terms; Compliant with BMS processes and SOPs, adherence to global and project standards within an indication or therapeutic area and responsible for quality of deliverable Fresh PhD or MS with 2+ 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
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