Senior Manager, Biostatistics

Role: Biostatistics lead supporting clinical studies within Gilead’s biopharma pipeline, focusing on trial design, analysis, and regulatory submissions. Responsibilities: oversee statistical analysis, review data for NDA submissions, develop analysis plans, provide statistical input in cross-functional team discussions, and lead technical activities for complex clinical trials. May manage projects or teams, contribute to methodology improvements, and support regulatory documentation. Requirements: PhD in biostatistics or related field with 4+ years (PhD) or 6+ years (MS) or 8+ years (BA/BS) relevant industry experience, expertise in biomedical data analysis using SAS, and experience managing projects or small teams. Preferred: proven leadership, advanced statistical knowledge, and experience with clinical trial data, safety analysis, and biomarker studies. High-Value: supporting clinical development, regulatory submissions, and data analysis for therapies addressing infectious diseases and oncology, with involvement in multiple study phases. Collaboration: internal cross-functional teams, external partners, and regulatory authorities. Work setup: not specified, but the role involves technical leadership and project oversight.