Tech Stack

Description

You will independently lead the design, analysis, and reporting for multiple oncology clinical trials, proposing efficient study designs and collaborating with cross-functional teams. Your work will drive adoption of Natera's molecular diagnostic tests.

Requirements

• Advanced degree in Biostatistics or Statistics (Ph.D. preferred)
• 4+ years experience in clinical trial biostatistics
• Expertise in time-to-event analysis and survival modeling
• Proficiency in R
• Knowledge of ICH, GCP, and CDISC standards

Responsibilities

• Lead statistical design and analytical planning for oncology clinical utility studies
• Serve as study statistician and collaborate with clinical, medical, and translational partners
• Author and review statistical analysis plans and reports
• Recommend and apply novel statistical approaches
• Mentor early career statisticians