Principal Statistical Analyst

Revolution Medicines seeks an experienced statistical programmer for late-stage oncology clinical trials, providing oversight and hands-on SAS support for RAS-targeted cancer therapies currently in development.

Key Responsibilities

• Effectively collaborate with cross-functional teams to provide programming timelines for various deliverables
• Deliver SAS technical guidance to the programming team
• Participate in internal and regulatory authority audits
• Manage timelines and vendors for regulatory submissions meeting FDA 21 CFR Part 11 standards
• Oversee programming for CDISC-compliant datasets, statistical plans, and regulatory documentation
• Execute hands-on programming for dose committees, board meetings, and exploratory analyses
• Conduct verification reviews of presentations and publications

Required Qualifications

• 14+ years statistical programming experience with oncology clinical trials
• BS/BA degree or equivalent field-relevant qualification
• Experience leading statistical programming contractors and vendors
• Proficiency with SAS for analysis datasets, tables, listings, and figures
• Demonstrated ability to multitask and execute goals on interdisciplinary teams

Preferred Qualifications

• Strong leadership and teamwork track record
• Background in small to mid-sized biotech/pharma settings
• Experience developing statistical programming processes, SOPs, and guidance documents

Compensation: $186,000 - $233,000 USD. Work arrangement: Hybrid (Redwood City, CA headquarters).