Senior Manager, Biostatistics

Position 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, advises 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, adheres to global and project standards within an indication or therapeutic area and is 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 requirements. Develops and advises team members. Effectively communicates the DQS Mission and Vision in a fashion that generates pride, excitement and commitment within DQS. 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. Compensation Overview Brisbane, CA, US: $188,730 – $228,701 Cambridge Crossing: $188,730 – $228,701 Princeton, NJ, US: $164,110 – $198,862 Seattle, WA: $180,520 – $218,751 The starting compensation range above for a full‑time employee (FTE) basis. Additional incentive cash and stock opportunities may be available based on eligibility. Final, individual compensation will be decided based on demonstrated experience. Benefits Our benefits include: Health Coverage (medical, pharmacy, dental, and vision care); Well‑Being Support (BMS Well‑Being Account, BMS Living Life Better, Employee Assistance Programs); Financial Well‑Being and Protection (401(k), disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, survivor support). Equal Employment Opportunity Visit to access our complete Equal Employment Opportunity statement. #J-18808-Ljbffr