Senior Biostatistics Manager: Trial Design & Analysis

Bristol-Myers Squibb Co; New Jersey; On-site; USD 140,000 - 180,000; Full time

Job summary

Bristol Myers Squibb is seeking a Senior Manager of Biostatistics to join cross-functional development teams in New Jersey. You will contribute to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.

You will collaborate with the Biostatistics Lead and other team members to ensure high-quality statistical deliverables, clear data interpretation, and compliant documentation across studies.

Qualifications

• Experience in biostatistics within drug development.
• Ability to design and interpret statistical analyses.
• Experience preparing regulatory submissions.

Responsibilities

• Collaborates in design of clinical study including methodology, data analysis & interpretation, and reporting of study results.
• Authors and/or reviews protocol synopsis, protocol, statistical analysis plans, case-report forms, clinical study reports, and other study level specification documents with minimum supervision.
• Performs and/or validates statistical analyses, and advises on maximizing clarity of data display.
• Communicates results to cross-functional teams and provides data interpretation in study documents such as clinical study reports and publications.

Skills

Biostatistics

Trial design

Protocol development

Analysis planning

Regulatory submissions

Job description

Bristol Myers Squibb is seeking a Senior Manager of Biostatistics to join cross-functional development teams in New Jersey. You will contribute to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.

You will collaborate with the Biostatistics Lead and other team members to ensure high-quality statistical deliverables, clear data interpretation, and compliant documentation across studies.