Principal Biostatistician Consultant

Providing statistical leadership for oncology clinical development programs, the remote Principal Biostatistician Consultant will manage Phase I-III clinical trials, develop statistical analysis plans, and collaborate with cross-functional teams to support regulatory submissions. Key Responsibilities Provide statistical leadership for oncology clinical trials across multiple phases (Phase I-III) Lead the development of statistical analysis plans (SAPs), protocols, and clinical study reports (CSRs) Collaborate with clinical development, data management, programming, regulatory, and medical teams Required Qualifications PhD or MS in Statistics, Biostatistics, or related field 8+ years (MS) or 6+ years (PhD) of industry experience in biostatistics Strong experience in oncology clinical trials Proficiency in SAS and/or R Strong knowledge of CDISC standards (SDTM, ADaM)