Principal Statistical Analyst Job at Revolution Medicines, Redwood City, CA

  • Revolution Medicines
  • Redwood City, CA

Job Description

Revolution Medicines seeks a Principal Statistical Analyst with 14+ years of experience in oncology clinical trial programming. The role involves leading statistical programming efforts across early and late-phase studies, overseeing regulatory submissions, and managing internal deliverables while ensuring CDISC compliance.

Responsibilities

  • Lead one or more early-phase or late-phase clinical studies and programming initiatives
  • Provide SAS programming technical support and guidance to programming team members
  • Oversee deliverables including regulatory submissions, datasets, and statistical analysis plans
  • Manage timelines and vendor performance for submission-related activities
  • Participate in internal and regulatory authority audits and compliance activities

Requirements

  • 14+ years statistical programming experience in early or late phase oncology trials
  • Bachelor's degree or equivalent qualification in relevant field
  • Experience leading statistical programming contractors and vendors
  • Hands-on SAS programming proficiency for analysis datasets and regulatory outputs
  • Ability to multitask, prioritize, and work effectively in interdisciplinary teams
  • Knowledge of FDA 21 CFR Part 11, GxP, and CDISC standards (SDTM, ADaM)

Job Tags

For contractors

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