Revolution Medicines is seeking a statistician to lead biostatistical activities and provide statistical expertise for design, analysis, and reporting of clinical studies in oncology.
Requirements
- Hands-on experience in design and analysis of oncology trials
- Solid knowledge in ICH and other regulatory requirements related to biostatistical activities and clinical trials
- Proficiency in SAS and/or R
- Hands-on experience in design and analysis of phase 3 oncology trials (desirable)
Responsibilities
- Represent biostatistics on study and cross-functional project teams, providing statistical leadership
- Lead and manage biostatistical activities to ensure consistency, scientific rigor, and timely deliverables
- Develop statistical analysis plans and analysis specifications; ensure analyses align with clinical and regulatory objectives
- Collaborate with statistical programming to ensure that analysis is conducted per statistical plan and specifications and delivered with high quality
- Collaborate with data management and clinical operations to ensure robust CRF and database development and quality data collection
- Provide statistical input to the development of global health authority documents, regulatory interaction and response to health authority submissions
- Influence strategy and inform decision-making through data-driven insights and clear communication of risk and benefit
Other
- Ph.D. or M.S. in Statistics/Biostatistics
- A minimum of 5 years (for Ph.D.) and 8 years (for M.S.) of experience in biotech/pharma industry as a statistician
- Ability to work independently and within a team
- Excellent verbal and written communication skills
- Good interpersonal and project management skills
