Senior 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 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. These individuals develop collaborative relationships and work effectively with the Biostatistics Lead and other cross functional team members.

Key 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.
• 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 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
• Organize multiple work assignments and establish priorities
• Experience in standard and advanced statistical methods is preferred.
• Good understanding of regulatory requirements & clinical trial design is preferred.

If you come across a role that intrigues you but doesnt perfectly line up with your resume we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work Life-changing Careers
With a single vision as inspiring as Transforming patients lives through science every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture promoting global participation in clinical trials while our shared values of passion innovation urgency accountability inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential site-by-design field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles onsite presence is considered an essential job function and is critical to collaboration innovation productivity and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application or in any part of the recruitment process direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff customers patients and communities. As a result the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

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

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