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What You'll Do:
- Design and review statistical methodology in protocols and statistical analysis plans.
- Lead execution of statistical analyses according to plans and exploratory analyses.
- Produce high-quality presentations and author documentation of analysis plans, methods, results, and interpretation.
What We're Looking For:
- Master's or PhD in biostatistics or statistics with relevant experience in regulated clinical trials.
- At least 3 years of practical experience designing and executing statistical analyses for regulatory submissions.
- Proficiency in statistical software such as R, SAS, or JMP.
What We Offer:
- Competitive benefits including medical, dental, vision, life, and disability plans.
- Free genetic testing for employees and immediate family, plus fertility care benefits.
- Pregnancy and baby bonding leave, 401k, commuter benefits, and generous employee referral program.
Natera
Natera is a global leader in cell-free DNA testing for oncology, women's health, and organ health. The team consists of highly dedicated professionals from world-class institutions who care deeply about their work and each other.