Sr. Manager

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. They develop collaborative relationships and work effectively with the Biostatistics Lead and other team members.

• Collaborate in the design of clinical studies, including methodology, data analysis, interpretation, and reporting of results.
• Author and/or review protocol synopsis, protocol, statistical analysis plans, case‑report forms, clinical study reports, associated publications, and other study‑level specification documents with minimal supervision.
• Perform or validate statistical analyses and advise on clarity of data display.
• Communicate results to cross‑functional teams and provide data interpretation in study documents such as clinical study reports and publications.
• Translate scientific questions into statistical terms and convert statistical concepts into layman terms.
• Ensure compliance with BMS processes and SOPs, adherence to global and project standards, and maintain quality of deliverables.
• Continuously develop technical knowledge of statistical methodology and application in trial design and data analysis for clear, concise, high‑quality results.
• Enhance knowledge of drug development, regulatory, and commercial requirements.
• Develop and advise team members.
• Communicate GBDS Mission and Vision in a manner that fosters pride, excitement, and commitment.
• Promote an inclusive culture that respects diversity, complies with processes, and encourages constructive questioning.

• Fresh PhD with 3+ years’ experience or MS with 5+ years’ 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.
• Strong interpersonal, communication, writing, and organizational skills.
• Ability to learn regulatory requirements and clinical trial design, work successfully within cross‑functional teams, and prioritize multiple work assignments.
• Preferred experience in standard and advanced statistical methods.
• Good understanding of regulatory requirements and clinical trial design.

Madison - Giralda - NJ - US: $164,110 - $198,862

Princeton - NJ - US: $164,110 - $198,862

The starting compensation range(s) for this role are listed above for a full‑time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. Final, individual compensation will be decided based on demonstrated experience.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.