Senior Biostatistics Manager – Clinical Trial Design

Bristol-Myers Squibb Co; Princeton (NJ); On-site; USD 164,000 - 199,000; Full time

Benefits offered by this job

Health Coverage

Wellbeing Programs

Financial Protection

Paid Time Off

Job summary

Bristol Myers Squibb Co in Princeton, NJ is seeking a Senior Manager, Biostatistics to join cross-functional development teams responsible for trial design, analysis planning, and regulatory submissions.

The role emphasizes collaboration with Biostatistics Leads, proficiency in SAS/R/Python, and delivering high-quality results under BMS standards, with competitive benefits and growth opportunities.

Qualifications

• Fresh PhD with 3+ years’ experience or MS with 5+ years’ experience in statistics or biostatistics or 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 & simulation.
• Good interpersonal, communication, writing and organizational skills

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, associated publications, and other study level specification documents with minimum supervision
• Performs and/or validates statistical analyses, advise ways to maximize clarity of data display
• Communicates results to cross-functional teams, provides data interpretation in study documents such as clinical study reports, and publications.
• Translates scientific questions into statistical terms and statistical concepts into layman terms.
• Compliant with BMS processes and SOPs, adherence to global and project standards within an indication or therapeutic area and responsible for quality of deliverable.
• Continually develops technical knowledge of statistical methodology and how it is appropriately applied in trial design and data analysis for clear, concise, high-quality results.
• Continually enhances knowledge of drug development process, regulatory and commercial requirement
• Develops & advises team members.
• Effectively communicates the DQS Mission and Vision in a fashion that generates pride, excitement and commitment within DQS

Skills

Statistical thinking

Cross-functional collaboration

Verbal written communication

Regulatory understanding

Education

Fresh PhD with 3+ years’ experience

MS with 5+ years’ experience

Tools

SAS

R

Python

Job description

Bristol Myers Squibb Co in Princeton, NJ is seeking a Senior Manager, Biostatistics to join cross-functional development teams responsible for trial design, analysis planning, and regulatory submissions.

The role emphasizes collaboration with Biostatistics Leads, proficiency in SAS/R/Python, and delivering high-quality results under BMS standards, with competitive benefits and growth opportunities.