Sr. Manager
Bristol Myers Squibb
June 30, 2026
Remote friendly (Princeton, NJ)
United States
Other
Position Summary
The Senior Manager of Biostatistics contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.
Key Responsibilities
- Collaborate in design of clinical studies (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 and/or validate statistical analyses; improve clarity of data display.
- Communicate results to cross-functional teams; provide interpretation in study documents and publications.
- Translate scientific questions into statistical terms and explain statistical concepts in lay terms.
- Ensure deliverables comply with BMS processes/SOPs and global/project standards; maintain quality.
- Develop technical statistical knowledge and enhance understanding of drug development/regulatory needs.
- Develop and advise team members; support an inclusive, respectful, compliant culture.
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 & simulation.
- Good interpersonal, communication, writing, and organizational skills.
- Ability to learn regulatory and clinical trial design/analysis; work cross-functionally; manage multiple assignments/priorities.
- Preferred: standard/advanced statistical methods experience; good regulatory and clinical trial design understanding.
Benefits (explicitly listed)
- Health coverage (medical, pharmacy, dental, vision)
- Wellbeing support programs (e.g., EAP)
- Financial protection (401(k), disability, life/accident/supplemental insurance, legal support, identity theft benefit)
- Paid time off and other leave options (as described)
Application Instruction
- Apply even if you don’t meet every requirement.
The Senior Manager of Biostatistics contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.
Key Responsibilities
- Collaborate in design of clinical studies (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 and/or validate statistical analyses; improve clarity of data display.
- Communicate results to cross-functional teams; provide interpretation in study documents and publications.
- Translate scientific questions into statistical terms and explain statistical concepts in lay terms.
- Ensure deliverables comply with BMS processes/SOPs and global/project standards; maintain quality.
- Develop technical statistical knowledge and enhance understanding of drug development/regulatory needs.
- Develop and advise team members; support an inclusive, respectful, compliant culture.
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 & simulation.
- Good interpersonal, communication, writing, and organizational skills.
- Ability to learn regulatory and clinical trial design/analysis; work cross-functionally; manage multiple assignments/priorities.
- Preferred: standard/advanced statistical methods experience; good regulatory and clinical trial design understanding.
Benefits (explicitly listed)
- Health coverage (medical, pharmacy, dental, vision)
- Wellbeing support programs (e.g., EAP)
- Financial protection (401(k), disability, life/accident/supplemental insurance, legal support, identity theft benefit)
- Paid time off and other leave options (as described)
Application Instruction
- Apply even if you don’t meet every requirement.