Bristol Myers Squibb
SeniorManager,Biostatistics
“Senior Manager, Biostatistics at Bristol Myers Squibb. Skills: Biostatistics, clinical trial design, statistical analysis, data interpretation, regulatory submissions, SAS, R, Python. Contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. Collaborates in design of clinical study including methodology, data analysis & interpretation, and reporting of study results”
What You'll Achieve.
preparation of regulatory submissions; quality of deliverable; clear, concise, high-quality results
Industry & Context.
Translates scientific questions into statistical terms
What They're Looking For.
Must Have
PhD with 3+ years’ experience or MS with 5+ years’ experience in statistics or biostatistics or related scientific field, Proficiency in scientific computing/programming (SAS, R or Python), implementation of advanced 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
Experience in standard and advanced statistical methods is preferred, Good understanding of regulatory requirements & clinical trial design is preferred
What You'll Do.
Contributes to trial design
interpretation of results
and preparation of regulatory submissions
Collaborates in design of clinical study including methodology
data analysis & interpretation
and reporting of study results
Authors and/or reviews protocol synopsis
statistical analysis plans
clinical study reports
associated publications
and other study level specification documents
Performs and/or validates statistical analyses
Advises ways to maximize clarity of data display
Communicates results to cross-functional teams
Provides data interpretation in study documents such as clinical study reports
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
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
Continually enhances knowledge of drug development process
regulatory and commercial requirement
Develops & advises team members
Effectively communicates the GBDS Mission and Vision
Enables a culture of inclusiveness
respect for diversity
compliance with process and allows for the questioning and challenging of others in a respectful and constructive manner
How You'll Work.
Team & Collaboration
member of cross-functional development teams; develop collaborative relationships and work effectively with the Biostatistics Lead, and other cross functional team members; work successfully within cross-functional teams; Communicates results to cross-functional teams
Communication Scope
Good interpersonal, communication, writing and organizational skills; Translates scientific questions into statistical terms and statistical concepts into layman terms; Communicates results to cross-functional teams
Process & Methodology
organize multiple work assignments and establish priorities
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