Senior Manager, Biostatistics
Bristol Myers Squibb
8 hours ago
Remote friendly (Madison, NJ)
United States
Clinical Research and Development
Position Summary
- Senior Manager, Biostatistics member of cross-functional development teams contributing to trial design, protocol development, analysis planning, interpretation of results, and 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 other study-level documents with minimum supervision.
- Perform/validate statistical analyses; advise on clear data display.
- Communicate results and data interpretations in study documents and publications.
- Translate scientific questions into statistical terms; statistical concepts into layman terms.
- Ensure compliance with BMS processes/SOPs and global/project standards; maintain quality of deliverables.
- Develop technical expertise in statistical methodology for trial design and data analysis.
- Enhance knowledge of drug development process and regulatory/commercial requirements.
- Develop and advise team members; communicate GBDS Mission/Vision; foster inclusiveness and respectful challenge.
Qualifications & Experience
- Fresh PhD (3+ years) or MS (5+ years) 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 & simulation.
- Strong interpersonal, communication, writing, and organizational skills.
Preferred
- Experience with standard and advanced statistical methods.
- Understanding of regulatory requirements and clinical trial design.
Benefits (explicit)
- Health coverage; wellbeing support; financial protection (e.g., 401(k), disability, life insurance).
- Paid time off (flexible/unlimited for US exempt; specified vacation/holidays for other groups).
- Senior Manager, Biostatistics member of cross-functional development teams contributing to trial design, protocol development, analysis planning, interpretation of results, and 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 other study-level documents with minimum supervision.
- Perform/validate statistical analyses; advise on clear data display.
- Communicate results and data interpretations in study documents and publications.
- Translate scientific questions into statistical terms; statistical concepts into layman terms.
- Ensure compliance with BMS processes/SOPs and global/project standards; maintain quality of deliverables.
- Develop technical expertise in statistical methodology for trial design and data analysis.
- Enhance knowledge of drug development process and regulatory/commercial requirements.
- Develop and advise team members; communicate GBDS Mission/Vision; foster inclusiveness and respectful challenge.
Qualifications & Experience
- Fresh PhD (3+ years) or MS (5+ years) 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 & simulation.
- Strong interpersonal, communication, writing, and organizational skills.
Preferred
- Experience with standard and advanced statistical methods.
- Understanding of regulatory requirements and clinical trial design.
Benefits (explicit)
- Health coverage; wellbeing support; financial protection (e.g., 401(k), disability, life insurance).
- Paid time off (flexible/unlimited for US exempt; specified vacation/holidays for other groups).