Tech Stack

Description

You will independently lead the design, analysis, and reporting for multiple practice-changing oncology clinical trials. You will propose efficient, fit-for-purpose study designs and collaborate with cross-functional teams to influence study planning and execution.

Requirements

• Advanced degree in Biostatistics, Statistics, or related quantitative field (Ph.D. preferred)
• 4+ years of experience in clinical trial biostatistics
• Strong expertise in time-to-event analysis, competing risks, and advanced survival modeling
• Expertise with innovative study designs (adaptive, biomarker-informed), power calculations, and endpoint evaluation
• Proficient in R; working knowledge of ICH/GCP guidelines and CDISC standards (SDTM, ADaM)

Responsibilities

• Lead statistical design and analytical planning for oncology clinical utility studies
• Provide technical expertise in complex study design methodologies and data analyses
• Serve as study statistician, collaborating with clinical, medical, and translational partners
• Author and review statistical deliverables including SAPs, TLFs, CSRs, and publications
• Recommend and apply novel statistical approaches, mentor early career statisticians