Senior Manager, Biostatistics

Bristol Myers Squibb • Princeton, NJ

8d • $148,230 - $206,567

About The Position

The Senior Manager of Biostatistics contributes to cross-functional development teams, supporting clinical trial design, protocol development, analysis planning, interpretation of results, and regulatory submissions. The role develops collaborative relationships and works effectively with the Biostatistics Lead and other cross-functional team members. The position also supports high-quality, compliant statistical deliverables and contributes to team members’ development.

Requirements

• Fresh PhD or MS with 2+ years of experience in statistics, biostatistics, or a related scientific field, with clinical trials, drug development, pharmaceutical industry, or healthcare experience.
• Proficiency in scientific computing/programming (SAS, R, or Python) and implementation of advanced statistical analysis, data manipulation, graphing, and simulation.
• Good interpersonal, communication, writing, and organizational skills.
• Ability to learn regulatory requirements and clinical trial design, data analysis, and interpretation.
• Ability to work successfully within cross-functional teams.
• Ability to organize multiple work assignments and establish priorities.

Nice To Haves

• Experience in standard and advanced statistical methods.
• Good understanding of regulatory requirements and clinical trial design.

Responsibilities

• Collaborate on clinical study design, including methodology, data analysis and interpretation, and reporting of study results.
• Author and/or review protocol synopses, protocols, statistical analysis plans, case-report forms, clinical study reports, associated publications, and other study-level specification documents, under some supervision.
• Perform and/or validate statistical analyses and advise on ways to maximize clarity of data displays.
• Communicate results to cross-functional teams and provide data interpretation in study documents and publications.
• Translate scientific questions into statistical terms and explain statistical concepts in lay terms.
• Follow BMS processes and SOPs, adhere to global and project standards within an indication or therapeutic area, and ensure the quality of deliverables.
• Continually develop technical knowledge of statistical methodology and its appropriate application in trial design and data analysis.
• Continually enhance knowledge of the drug development process and regulatory and commercial requirements.
• Develop and advise team members.
• Communicate the DQS Mission and Vision in a way that generates pride, excitement, and commitment within DQS.

Benefits

• Comprehensive benefit plans, including wellbeing support, retirement and financial protection benefits, and medical, dental, vision, life, and disability insurance offerings.
• Eligible U.S.-based exempt employees receive Flexible Time Off without a set accrual limit, subject to manager approval, and 11 paid company holidays annually.
• Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires, subject to manager approval, 11 paid company holidays, and 3 optional holidays.
• Depending on eligibility, additional time-off benefits may include paid sick leave, up to two paid volunteer days per year, summer-hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs.
• Eligible employees receive an annual Global Shutdown between Christmas Day and New Year's Day.
• Potential eligibility for additional discretionary incentive cash and stock opportunities.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior