Senior Manager, Biostatistics

Role: Biostatistics lead supporting clinical studies and non-molecule projects within Gilead's biopharma portfolio. Responsibilities include statistical analysis, study design consultation, authoring analysis plans, overseeing technical activities, and contributing to NDA submissions. The role involves cross-functional collaboration on trial design, data analysis, safety monitoring, and regulatory documentation. It may also entail leading projects related to statistical tools and methods. Requirements: PhD (preferred) or MS/BA with 4+ to 8+ years' industry experience, expertise in biomedical data analysis using SAS, and proven project/team management skills. High-value: supports clinical development across infectious diseases, oncology, and other therapeutic areas; involved in preclinical, IND, or phase 1-3 trials; may include biomarker and safety analyses. The position offers matrix management, regulatory compliance, and potential leadership in special projects. Work setup is not specified, but the emphasis on collaboration and project oversight indicates a dynamic, cross-functional environment.