Revolution Medicines Benefits Overview

The role involves overseeing statistical programming for oncology trials, providing guidance on regulatory submissions, managing cross-functional collaboration, and ensuring compliance with CDISC standards, while also leading programming teams and projects.

The Director of Analytical Development will lead analytical strategies for small molecule AP and drug product development, overseeing regulatory compliance, cross-functional collaborations, and quality management of external partners.

The Associate Director will oversee statistical programming for clinical trials in oncology, manage programming teams, ensure regulatory compliance, and lead project delivery timelines while providing hands-on SAS programming support.