Senior Manager, Biostatistics
Bristol Myers Squibb
September 02, 2026
Remote friendly (Princeton, NJ)
United States
Clinical Research and Development
Position Summary
Senior Manager of Biostatistics on cross-functional development teams contributing to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.
Key Responsibilities
- Collaborates in design of clinical studies (methodology, data analysis/interpretation, reporting).
- Authors and/or reviews protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, publications, and other study-level specifications with minimum supervision.
- Performs/validates statistical analyses; advises to maximize clarity of data display.
- Communicates results to cross-functional teams; provides data interpretation in study documents and publications.
- Translates scientific questions to statistical terms and concepts to layman terms.
- Ensures compliance with BMS processes/SOPs, global/project standards; delivers quality outputs.
- Continually develops technical/statistical methodology knowledge; enhances understanding of drug development, regulatory, and commercial requirements.
- Develops and advises team members; effectively communicates DQS Mission/Vision.
Qualifications & Experience
- Fresh PhD with 3+ years’ experience OR MS with 5+ years’ experience in statistics/biostatistics or related field with clinical trials/drug development/pharma/healthcare.
- Proficiency in SAS, R, or Python; advanced statistical analysis, data manipulation, graphing, simulation.
- Good interpersonal, communication, writing, and organizational skills.
Ability To
- Learn regulatory requirements and clinical trial design; work in cross-functional teams; organize multiple assignments/prioritize.
- Experience with standard/advanced statistical methods and understanding regulatory requirements are preferred.
Benefits (high level)
- Health coverage (medical/pharmacy/dental/vision); wellbeing support; 401(k) and insurance/disability benefits.
- Paid time off.
Application instruction
If you don’t perfectly match the resume, apply anyway.
Senior Manager of Biostatistics on cross-functional development teams contributing to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.
Key Responsibilities
- Collaborates in design of clinical studies (methodology, data analysis/interpretation, reporting).
- Authors and/or reviews protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, publications, and other study-level specifications with minimum supervision.
- Performs/validates statistical analyses; advises to maximize clarity of data display.
- Communicates results to cross-functional teams; provides data interpretation in study documents and publications.
- Translates scientific questions to statistical terms and concepts to layman terms.
- Ensures compliance with BMS processes/SOPs, global/project standards; delivers quality outputs.
- Continually develops technical/statistical methodology knowledge; enhances understanding of drug development, regulatory, and commercial requirements.
- Develops and advises team members; effectively communicates DQS Mission/Vision.
Qualifications & Experience
- Fresh PhD with 3+ years’ experience OR MS with 5+ years’ experience in statistics/biostatistics or related field with clinical trials/drug development/pharma/healthcare.
- Proficiency in SAS, R, or Python; advanced statistical analysis, data manipulation, graphing, simulation.
- Good interpersonal, communication, writing, and organizational skills.
Ability To
- Learn regulatory requirements and clinical trial design; work in cross-functional teams; organize multiple assignments/prioritize.
- Experience with standard/advanced statistical methods and understanding regulatory requirements are preferred.
Benefits (high level)
- Health coverage (medical/pharmacy/dental/vision); wellbeing support; 401(k) and insurance/disability benefits.
- Paid time off.
Application instruction
If you don’t perfectly match the resume, apply anyway.