Senior/Principal Statistician Consultant - Phase III Oncology (Remote)

📋 Description Provide statistical expertise and hands-on support for Phase III oncology clinical trials Contribute to study design, statistical analysis, interpretation of results, and clinical study Demonstrate a strong understanding of key oncology endpoints, including OS, PFS, ORR, and DoR Apply appropriate methods for censoring and time-to-event analyses Apply and interpret statistical methodologies including Kaplan-Meier analysis, Cox Proportional Author, review, and provide input into TFL and ADaM specifications in close collaboration with 🎯 Requirements Advanced degree (MS, PhD, or equivalent) in Statistics, Biostatistics, or a related quantitative Direct hands-on experience supporting at least one Phase III oncology clinical trial Strong understanding of oncology clinical trial endpoints, including OS, PFS, ORR, and DoR Strong knowledge of censoring rules and time-to-event analysis Hands-on experience with Kaplan-Meier, Cox Proportional Hazards, and stratified log-rank methods Strong SAS programming skills with the ability to review statistical programming outputs and 🎁 Benefits Preferred qualifications: Experience supporting FDA and/or EMA regulatory submissions Preferred qualifications: Experience with IDMC/DMC activities and interim analyses, including Preferred qualifications: Experience with R programming is a plus Preferred qualifications: Experience working in a CRO, pharmaceutical, or biotechnology environment