Director, Biostatistics, Early Phase
$211,000–$264,000 year
HybridRedwood City, California, United States
Job Summary
Lead statistical analysis for oncology studies, including design, analysis, and reporting of clinical trials. Represent biostatistics on study teams to collaborate on protocol development, statistical methodology, and analysis specifications. Develop statistical analysis plans and specifications while ensuring analysis aligns with statistical plans. Partner with data management and clinical operations to ensure robust database development and quality data collection. Provide statistical input for regulatory interactions and health authority submissions. Contribute to publications, assist in data interpretation, and develop functional-level standards, SOPs, and templates. Maintain expertise in advanced statistical methods and share knowledge across the team.
Required Qualifications
- Ph.D. or M.S. in Statistics/Biostatistics
- 8 years of experience in biotech/pharma industry as a statistician for clinical trials (for Ph.D.)
- 12 years of experience in biotech/pharma industry as a statistician for clinical trials (for M.S.)
- Hands-on experience in design and analysis of oncology trials
- Ability to work independently and within a team
- Ability to apply statistical knowledge to solve real-world problems and acquire new knowledge in advanced statistical methods (e.g., Bayesian methods, predictive modeling etc.)
- Excellent verbal and written communication skills
- Good interpersonal and project management skills
- Proficiency in SAS and/or R
- Must be available for onsite work at headquarters in Redwood City, CA
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