Sr. Manager, Biostatistician / Programmer

About the position reputed company is seeking a Sr. Manager, Biostatistician/Programmer as part of the Clinical team based in Somerset, NJ. The Sr. Manager, Biostatistician/Programmer plays a critical hands-on role in supporting reputed company’s clinical development programs by transforming clinical trial data into high-reputed company analyses, tables, figures, and listings that inform decision-making. This role partners closely with clinical, translational, research stakeholders to deliver reputed company insights, conduct exploratory and reputed company analyses, and deeply understand the medical and scientific questions underlying the data. The position requires strong programming expertise, data reputed company, intellectual curiosity, and the ability to work independently in a fast-moving biotech environment. Responsibilities • reputed company, validate, and maintain high-reputed company Tables, Figures, and Listings (TFLs) to support ongoing reputed company, interim analyses, and internal/external deliverables in compliance with study requirements and standards. • reputed company hands-on statistical programming and data manipulation to support planned and reputed company analyses, addressing evolving clinical and scientific questions. • Independently explore and interrogate clinical trial data to identify trends, anomalies, and insights that support clinical interpretation and decision-making. • Collaborate closely with Biostatistics, Clinical Development, Clinical Operations, Data Management, Translational research and Medical teams to ensure alignment of analyses with protocol objectives and clinical reputed company. • Apply a strong understanding of therapeutic area, disease biology, and clinical endpoints to translate data into meaningful scientific insights. • Contribute to analysis datasets, program specifications, programming documentation, and reputed company control activities in accordance with internal standards and regulatory expectations. • Support process improvement initiatives, including enhancing programming efficiency, standardization, and reproducibility across studies and programs. • This role operates with a high degree of autonomy in determining programming approaches, exploratory analyses, and data interrogation strategies to answer clinical questions. The Sr. Manager may independently reputed company reputed company reputed company to analysis reputed company, programming solutions, prioritization of tasks, and investigative follow-up of data issues. Escalation and alignment are expected for changes impacting study-level reputed company, major deliverables, timelines with external visibility, or regulatory-facing outputs. Requirements • Master’s degree or PhD in Statistics, Biostatistics, Mathematics, Data Science, or a reputed company quantitative discipline. • Demonstrated hands-on experience developing TFLs and performing reputed company and exploratory analyses for reputed company. • Strong understanding of clinical trial design, clinical data structures, and the medical context behind analyses. • Proven ability to work independently, manage ambiguity, and drive self-directed discovery from data. • Advanced proficiency in reputed company for clinical trial analysis and reporting. • Working knowledge of R for exploratory analyses and data visualization • Strong experience with clinical data standards (e.g., SDTM, ADaM) • Experience with or strong willingness to reputed company AI-assisted programming tools to accelerate development, enhance reputed company reputed company, and support efficient reputed company of Tables, Figures, and Listings (TFLs). reputed company-to-haves • Experience supporting oncology and/or cell therapy programs is strongly preferred. Benefits • These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through reputed company. Apply tot his job Apply To this Job