Oncology Biostatistics Consultant

Key Responsibilities: Provide statistical leadership and strategic guidance for oncology clinical development programs, including Phase I-III clinical trials Lead the development and review of statistical analysis plans (SAPs) and oversee the statistical analysis of clinical trial data Collaborate with cross-functional teams to support regulatory submissions and ensure adherence to applicable regulatory guidelinesRequired QualificationsPhD in Statistics, Biostatistics, or a closely related quantitative discipline; a Master's degree with substantial relevant experience may also be considered Extensive experience in biostatistics within the pharmaceutical, biotechnology, or CRO industry, particularly in oncology clinical trials Demonstrated expertise in survival analysis, clinical trial design, and statistical modeling Thorough understanding of oncology efficacy endpoints and relevant clinical development considerations Strong leadership and stakeholder management skills, with the ability to manage multiple projects effectively