Associate Director, Biostatistics

Role: Associate Director of Biostatistics at RayzeBio, focusing on designing, executing, and interpreting statistical analyses for clinical oncology trials involving radiopharmaceuticals. Responsibilities include leading biostatistics strategies, collaborating with multidisciplinary teams, authoring key statistical documents (e.g., SAPs, protocols), reviewing vendor deliverables, supporting regulatory submissions, and exploring AI applications to enhance processes. Requirements: PhD or MS in Statistics/Biostatistics; 6+ years (PhD) or 8+ years (MS) of industry experience; expertise in biostatistical methodologies, regulatory guidelines (GCP, ICH), and familiarity with programming tools (SAS, R) and CDISC standards. Preferred: oncology clinical development background and experience with global regulatory filings. High-Value: Oncology, radiopharmaceutical modality, clinical trial phases, regulatory interactions, GxP compliance, cross-functional collaboration, potential AI integration. Work setup: Remote U.S.; ~10% travel; evening/weekend flexibility.