Senior Manager, Biostatistics
Bristol Myers Squibb
5 days ago
Remote friendly (Madison, NJ)
United States
Clinical Research and Development
Position Summary
The Senior Manager of Biostatistics is a member of cross-functional development teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.
Key Responsibilities
- Collaborates in design of clinical study (methodology, data analysis/interpretation, reporting).
- Authors and/or reviews protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, and related study specification documents.
- Performs and/or validates statistical analyses; advises on clear data display.
- Communicates results and provides data interpretation for study documents and publications.
- Translates scientific questions into statistical terms and explains concepts for non-statistical audiences.
- Ensures compliance with BMS processes/SOPs and global/project standards; maintains deliverable quality.
- Develops technical expertise in statistical methodology and drug development/regulatory requirements.
- Develops and advises team members; supports inclusive, respectful team culture.
Qualifications & Experience
- Fresh PhD with 3+ years’ experience OR MS with 5+ years’ experience in statistics/biostatistics (clinical trials/drug development/pharma/healthcare preferred).
- Proficiency in SAS, R or Python; advanced statistical analysis, data manipulation, graphing, and simulation.
- Strong interpersonal, communication, writing, and organizational skills.
- Preferred: standard/advanced statistical methods; understanding of regulatory requirements and clinical trial design.
Benefits (examples)
- Health coverage (medical/pharmacy/dental/vision), wellbeing support, 401(k), disability/life insurance.
- Paid time off (varies by location/role eligibility).
Application Instructions
- Apply even if the role doesn’t perfectly match your resume.
The Senior Manager of Biostatistics is a member of cross-functional development teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.
Key Responsibilities
- Collaborates in design of clinical study (methodology, data analysis/interpretation, reporting).
- Authors and/or reviews protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, and related study specification documents.
- Performs and/or validates statistical analyses; advises on clear data display.
- Communicates results and provides data interpretation for study documents and publications.
- Translates scientific questions into statistical terms and explains concepts for non-statistical audiences.
- Ensures compliance with BMS processes/SOPs and global/project standards; maintains deliverable quality.
- Develops technical expertise in statistical methodology and drug development/regulatory requirements.
- Develops and advises team members; supports inclusive, respectful team culture.
Qualifications & Experience
- Fresh PhD with 3+ years’ experience OR MS with 5+ years’ experience in statistics/biostatistics (clinical trials/drug development/pharma/healthcare preferred).
- Proficiency in SAS, R or Python; advanced statistical analysis, data manipulation, graphing, and simulation.
- Strong interpersonal, communication, writing, and organizational skills.
- Preferred: standard/advanced statistical methods; understanding of regulatory requirements and clinical trial design.
Benefits (examples)
- Health coverage (medical/pharmacy/dental/vision), wellbeing support, 401(k), disability/life insurance.
- Paid time off (varies by location/role eligibility).
Application Instructions
- Apply even if the role doesn’t perfectly match your resume.