Associate Director, Biostatistics – Early Phase

Revolution Medicines

Redwood City, California, United States
Base: $186,000 - $233,000 usd; bonus/equity: compe...
On-site
Hands-on experience in design and analysis of oncology trials
Proficiency in sas and/or r statistical software
Ability to apply advanced statistical methods like bayesian
Revolution Medicines is seeking an Associate Director of Biostatistics for their oncology studies in Redwood City, California. The ideal candidate will have significant experience in clinical trial statistics, particularly within oncology, and will play a key role in study design, analysis, and regulatory interactions

Job Summary

  • Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers.
  • This position serves as a study level statistician responsible for the design, analysis, and reporting of oncology clinical studies.
  • The role requires collaboration with cross-functional teams including data management, clinical operations, and regulatory affairs to ensure robust data collection and submission quality.

Matching Summary

Match Score: 85

Revolution Medicines is seeking an Associate Director of Biostatistics for their oncology studies in Redwood City, California. The ideal candidate will have significant experience in clinical trial statistics, particularly within oncology, and will play a key role in study design, analysis, and regulatory interactions.

Salary

Base: $186,000 - $233,000 USD; Bonus/Equity: Competitive cash compensation and robust equity awards; Benefits: Strong benefits and significant learning opportunities

Skills & Requirements

Must-have

  • Hands-on experience in design and analysis of oncology trials
  • Proficiency in SAS and/or R statistical software
  • Ability to apply advanced statistical methods like Bayesian

Nice-to-have

  • Excellent verbal and written communication skills
  • Strong interpersonal and project management skills
  • Experience developing functional-level standards and SOPs

Key Requirements

  • Ph.D. or M.S. in Statistics/Biostatistics
  • Minimum 5 years (Ph.D.) or 8 years (M.S.) biotech/pharma industry experience
  • Must have hands-on experience in oncology trial design and analysis

Work Rights

Not specified

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