Sr. Manager
Bristol Myers Squibb
August 22, 2026
Remote friendly (Princeton, NJ)
United States
Other
Position Summary
The Senior Manager of Biostatistics is part of cross-functional development teams contributing to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.
Key Responsibilities
- Collaborate on clinical study design (methodology, data analysis/interpretation, reporting).
- Author/review protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, publications, and related specification documents with minimal supervision.
- Perform/validate statistical analyses; advise on clear data display.
- Communicate results and provide data interpretation for study documents and publications.
- Translate scientific questions to statistical terms and explain statistical concepts to non-statisticians.
- Ensure compliance with BMS processes/SOPs and global/project standards; maintain deliverable quality.
- Develop technical knowledge of statistical methodology; enhance knowledge of drug development and regulatory/commercial requirements.
- Develop and advise team members; enable a culture of candor.
Qualifications & Experience
- Fresh PhD with 3+ years’ experience or MS with 5+ years’ experience in statistics/biostatistics (or related) with clinical trials/drug development/pharma or healthcare experience.
- Proficiency in SAS, R, or Python for advanced statistical analysis, data manipulation, graphing, and simulation.
- Strong interpersonal, communication, writing, and organizational skills.
Preferred
- Experience with standard/advanced statistical methods.
- Understanding of regulatory requirements and clinical trial design.
Benefits (explicit)
- Health coverage (medical/pharmacy/dental/vision), wellbeing support, 401(k), and insurance/disability.
Application instructions
- If you’re interested but don’t perfectly match, you’re encouraged to apply.
The Senior Manager of Biostatistics is part of cross-functional development teams contributing to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.
Key Responsibilities
- Collaborate on clinical study design (methodology, data analysis/interpretation, reporting).
- Author/review protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, publications, and related specification documents with minimal supervision.
- Perform/validate statistical analyses; advise on clear data display.
- Communicate results and provide data interpretation for study documents and publications.
- Translate scientific questions to statistical terms and explain statistical concepts to non-statisticians.
- Ensure compliance with BMS processes/SOPs and global/project standards; maintain deliverable quality.
- Develop technical knowledge of statistical methodology; enhance knowledge of drug development and regulatory/commercial requirements.
- Develop and advise team members; enable a culture of candor.
Qualifications & Experience
- Fresh PhD with 3+ years’ experience or MS with 5+ years’ experience in statistics/biostatistics (or related) with clinical trials/drug development/pharma or healthcare experience.
- Proficiency in SAS, R, or Python for advanced statistical analysis, data manipulation, graphing, and simulation.
- Strong interpersonal, communication, writing, and organizational skills.
Preferred
- Experience with standard/advanced statistical methods.
- Understanding of regulatory requirements and clinical trial design.
Benefits (explicit)
- Health coverage (medical/pharmacy/dental/vision), wellbeing support, 401(k), and insurance/disability.
Application instructions
- If you’re interested but don’t perfectly match, you’re encouraged to apply.