Manager, Biostatistics

Working with Us
Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthroughs in cell therapy this is work that transforms the lives of patients and the careers of those who do it. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits services and programs that provide our employees with the resources to pursue their goals both at work and in their personal lives. Read more: Summary
The Manager of Biostatistics is a member of cross-functional study/project teams and contributes to trial design protocol development analysis planning interpretation of results and preparation of regulatory submissions. These individuals develop collaborative relationships and work effectively with the Biostatistics Lead and other cross functional team members.

Key Responsibilities

• Contributes to designing clinical trials to address study hypotheses and objectives.

• Authors and/or reviews protocol synopsis protocol statistical analysis plan data presentation plan case-report forms clinical study reports associated publications and other study level specification documents under supervision.

• Performs and/or validates preplanned or ad hoc statistical analyses with guidance as needed.

• Presents & interprets results to GBDS and/or cross-functional team members.

• 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.

• Effectively communicates the GBDS Mission and Vision in a fashion that generates pride excitement and commitment within GBDS.

• Enables a culture of inclusiveness respect for diversity compliance with process and allows for the questioning and challenging of others in a respectful and constructive manner.

Qualifications & Experience

• Fresh MS in statistics or biostatistics or related scientific field preferred.

• Proficiency in scientific computing/programming (SAS R or Python) and implementation of 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

• organize multiple work assignments and establish priorities