Bristol Myers Squibb
Manager,Biostatistics
“Manager, Biostatistics at Bristol Myers Squibb. Skills: Biostatistics, statistical analysis, clinical trials, drug development. Contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. Contributes to designing clinical trials to address study hypotheses and objectives”
What You'll Achieve.
preparation of regulatory submissions; clear, concise, high-quality results
Industry & Context.
Translates scientific questions into statistical terms
On-site Protocol: Site-essential, site-by-design, field-based and remote-by-design jobs. Occupancy type determined by the nature and responsibilities of your role., Ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function for field-based and remote-by-design roles.
What They're Looking For.
Must Have
MS in statistics, or biostatistics or related scientific field with 1-2 years’ experience in clinical trials, drug development, pharmaceutical industry or healthcare experience, Proficiency in scientific computing/programming (SAS, R or Python) and implementation of statistical analysis, data manipulation, graphing & simulation, Good interpersonal, communication, writing and organizational skills, Ability to learn regulatory requirements & clinical trial design, data analysis and interpretation, Ability to work successfully within cross-functional teams, Ability to organize multiple work assignments and establish priorities
Nice to Have
fresh Ph. D in Statistics with Biostatistics relevant coursework (including internship) preferred
What You'll Do.
Contributes to trial design
interpretation of results
and preparation of regulatory submissions
Contributes to designing clinical trials to address study hypotheses and objectives
Authors and/or reviews protocol synopsis
statistical analysis plan
data presentation plan
clinical study reports
associated publications
and other study level specification documents under supervision
Performs and/or validates preplanned or ad hoc statistical analyses with guidance as needed
Presents & interprets results to GBDS and/or cross-functional team members
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
Continually develops technical knowledge of statistical methodology and how it is appropriately applied in trial design and data analysis for clear
How You'll Work.
Team & Collaboration
member of cross-functional study/project teams; develops collaborative relationships and work effectively with the Biostatistics Lead, and other cross functional team members; work successfully within cross-functional teams
Communication Scope
communication; writing; Translates scientific questions into statistical terms and statistical concepts into layman terms
Process & Methodology
organize multiple work assignments and establish priorities
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