Job Description: • Lead the statistical design and analytical planning for oncology clinical utility studies. • Serve as study statistician for multiple studies. • Author and review high-quality statistical deliverables, including statistical analysis plans (SAPs), and reports (TLFs, CSRs, publications). • Recommend and apply novel statistical approaches where appropriate. Requirements: • Advanced degree in Biostatistics, Statistics, or a related quantitative field (Ph.D. preferred). • 7+ years of experience in clinical trial biostatistics. • Strong expertise in time-to-event analysis, including handling of censoring, competing risks, and advanced survival modeling approaches commonly used in oncology. • Expertise with innovative study design (e.g. adaptive and biomarker-informed designs), power calculations, and endpoint evaluation. • Working knowledge of ICH and GCP guidelines as well as CDISC standards (e.g. SDTM, ADaM). • Proficient in R. Benefits: • Comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. • Free testing for employees and their immediate families, in addition to fertility care benefits. • Pregnancy and baby bonding leave. • 401k benefits. • Commuter benefits. • Generous employee referral program!