Associate Principal Statistical Analyst

Revolution Medicines seeks an experienced statistical programmer to support oncology clinical trials involving RAS-targeted therapeutics, combining hands-on programming with team oversight and regulatory submission guidance. This is requisition P2223, requiring 14+ years of experience.

Key Responsibilities

• Collaborate across teams to establish programming timelines for deliverables
• Deliver SAS programming technical support and guidance to programming staff
• Participate in internal and regulatory authority audits
• Manage vendor timelines and ensure conformance to CDISC standards and submission guidelines
• Oversee programming for regulatory submissions, publications, and CDISC datasets
• Execute hands-on programming for dose committees and exploratory analyses
• Review and verify documents for internal presentations and external publications

Required Qualifications

• 14+ years statistical programming experience in early or late phase oncology trials
• BS/BA degree or equivalent qualification in relevant field
• Experience leading statistical programming contractors and vendors
• Proficiency in SAS programming for analysis datasets, tables, listings, and figures
• Demonstrated multitasking ability and collaborative team skills

Preferred Qualifications

• Strong demonstrated leadership and teamwork record
• Small to mid-sized biotech/pharma environment experience
• Experience developing processes, SOPs, and guidance documents for statistical programming

Compensation: $164,000 - $205,000 USD. Work arrangement: Hybrid (Redwood City, CA headquarters).