Senior Biostatistics Manager — Clinical Trials & Data Insights

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

Benefits offered by this job

Flexible Time Off

11 company holidays

Paid vacation 160 hours

Stock opportunities

Four work models

Comprehensive benefits

Job summary

Bristol Myers Squibb EU Policy is seeking a Senior Manager of Biostatistics to join cross-functional development teams. You will contribute to trial design, protocol development, analysis planning, and regulatory submissions, collaborating closely with the Biostatistics Lead and other team members.

The role emphasizes translating scientific questions into statistical terms, ensuring quality through BMS processes, and advancing knowledge in statistical methods and drug development.

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
• Ability to learn regulatory requirements & clinical trial design, data analysis and interpretation
• Work successfully within cross-functional teams and organize multiple priorities
• Experience in standard and advanced statistical methods is preferred
• Good understanding of regulatory requirements & clinical trial design is preferred

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 GBDS Mission and Vision in a fashion that generates pride, excitement and commitment within GBDS
• Enable a culture of candor; respect of process which allows for the questioning and challenging of others in a respectful and constructive manner

Skills

Statistical analysis

Data manipulation

Graphing & simulation

SAS

R

Python

Interpersonal skills

Writing and communication

Education

PhD in statistics/biostatistics or related

MS in statistics/biostatistics or related

Tools

SAS

R

Python

Job description

Bristol Myers Squibb EU Policy is seeking a Senior Manager of Biostatistics to join cross-functional development teams. You will contribute to trial design, protocol development, analysis planning, and regulatory submissions, collaborating closely with the Biostatistics Lead and other team members.

The role emphasizes translating scientific questions into statistical terms, ensuring quality through BMS processes, and advancing knowledge in statistical methods and drug development.