Senior Manager RWE Biostats

At Bristol Myers Squibb our employees often ask Who are you working fora question that fuels collaboration accountability and urgency in our work. Our purpose-driven culture inspires us to discover develop and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work opportunities for growth and a supportive environment that values inclusion wellbeing flexibility and comprehensive benefits. This is work that transforms the lives of patients and the careers of those who do it.

The Senior Manager of RWE Biostatistics is a member of cross-functional teams and contributes to study design protocol/SAP development analysis planning interpretation of results and preparation of regulatory individuals develop collaborative relationships andwork effectively with the Biostatistics Leadand other cross functional team members.

Position Summary

Collaborates in design of RWE study including methodology data analysis & interpretation and reporting of study results.

Authors and/or reviews protocol statistical analysis plans study reports associated publications and other study level specification documents under some 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 real-world evidence generation related statistical methodology and how it is appropriately applied in study 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.

Education / Experience Requirements:

Fresh PhD or MS with 2 years experience in statistics or biostatistics or related scientific field with clinical trials and/or RWE in pharmaceutical industry or healthcare experience

Key Competency Requirements:

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.

We hire for skills and capabilities not just credentials if this role excites you but doesnt perfectly match your resume we encourage you to apply anyway.

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully carefully considering the nature of the role required skills work location schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors and individual team or Company performance.

Benefits:

Subject to the terms and conditions of the applicable plans then in effect you may be eligible to participate in our comprehensive benefit plans including wellbeing support retirement and financial protection benefits and insurance offerings (medical dental vision life and disability).

U.S.-based exempt employees are eligible for Flexible Time Off (FTO) which provides paid time off without a set accrual limit subject to manager approval along with 11 paid company holidays each year.

Non-exempt employees RayzeBio employees and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval) 11 paid company holidays and 3 optional holidays.

Depending on eligibility employees may also have access to additional time-off benefits including paid sick leave up to two paid volunteer days per year summer hours flexibility and leaves of absence for medical personal parental caregiver bereavement or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Years Day.

U.S.-based job seekers can explore full benefit offerings at We Work

Where you work matters because collaboration innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential site-by-design field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at People with Disabilities

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