Associate Director, Statistical Programming

Revolution Medicines seeks an experienced statistical programmer to support clinical oncology programs. The role combines hands-on programming with oversight of deliverables and regulatory submissions for RAS-targeted cancer therapies.

Key Responsibilities

• Collaborate with cross-functional teams on programming timelines
• Provide SAS programming technical guidance to team members
• Oversee internal and regulatory audits
• Manage vendors and timelines for regulatory submissions per FDA 21 CFR Part 11
• Lead production of CDISC-compliant datasets (SDTM, ADaM) and regulatory documentation
• Hands-on programming for exploratory analyses and committee presentations
• Review and verify documents for internal presentations and publications

Required Qualifications

• 14+ years statistical programming experience with early or late-phase oncology trials
• BS/BA degree or equivalent relevant qualification
• Experience leading programming contractors and vendors
• Proficiency in SAS for analysis datasets, tables, listings, and figures
• Ability to multitask, prioritize, and work effectively in interdisciplinary teams

Preferred Qualifications

• Demonstrated strong leadership and teamwork record
• Experience in small-to-mid-sized biotech/pharma companies
• Background developing processes, SOPs, and guidance for statistical programming functions

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