Associate Director, Biostatistics - Early Phase

Revolution Medicines seeks a statistician to serve as study-level analyst for oncology clinical trials, coordinating across functional groups to ensure timely completion of deliverables for RAS-targeted cancer therapies.

Key Responsibilities

• Represent biostatistics on study and project teams
• Provide statistical expertise for design, analysis and reporting of clinical studies
• Develop statistical analysis plans and specifications
• Collaborate with statistical programming to ensure that analysis is conducted per statistical plan
• Engage with data management and clinical operations on CRF and database development
• Support regulatory submissions with statistical input
• Contribute to publications and data interpretation consistency

Required Qualifications

• Ph.D. or M.S. in Statistics/Biostatistics (minimum 5 years pharma experience for Ph.D.; 8 years for M.S.)
• Demonstrated hands-on experience designing and analyzing oncology trials
• Proficiency in SAS and/or R
• Ability to work independently and collaboratively
• Excellent verbal and written communication skills
• Strong project management and interpersonal abilities

Preferred Qualifications

• Knowledge of advanced statistical methods including Bayesian approaches
• Experience with predictive modeling
• Familiarity with regulatory guidance and drug development processes

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