Senior Manager, Biostatistics
Bristol Myers Squibb
9 hours 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 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 and/or review protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, publications, and study specification documents.
- Perform/validate statistical analyses; advise on data display clarity.
- Communicate results and provide data interpretation in clinical study reports and publications.
- Translate scientific questions into statistical terms; explain statistical concepts in layman terms.
- Ensure compliance with BMS processes/SOPs and quality of deliverables.
- Develop technical expertise in statistical methodology and its use in trial design/data analysis.
- Enhance knowledge of drug development, regulatory, and commercial requirements.
- Develop and advise team members; communicate GBDS Mission/Vision; enable inclusive, respectful challenge.
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 experience.
- Proficiency in SAS, R, or Python; 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; wellbeing support; 401(k) and insurance benefits; Paid Time Off (unlimited flexible time for US Exempt; 160 hours annual paid vacation for certain roles).
Application
- If a role intrigues you but doesn’t perfectly match your resume, apply anyway.
The Senior Manager of Biostatistics is a member 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 and/or review protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, publications, and study specification documents.
- Perform/validate statistical analyses; advise on data display clarity.
- Communicate results and provide data interpretation in clinical study reports and publications.
- Translate scientific questions into statistical terms; explain statistical concepts in layman terms.
- Ensure compliance with BMS processes/SOPs and quality of deliverables.
- Develop technical expertise in statistical methodology and its use in trial design/data analysis.
- Enhance knowledge of drug development, regulatory, and commercial requirements.
- Develop and advise team members; communicate GBDS Mission/Vision; enable inclusive, respectful challenge.
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 experience.
- Proficiency in SAS, R, or Python; 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; wellbeing support; 401(k) and insurance benefits; Paid Time Off (unlimited flexible time for US Exempt; 160 hours annual paid vacation for certain roles).
Application
- If a role intrigues you but doesn’t perfectly match your resume, apply anyway.