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Primary Responsibilities:
- Lead biostatistics efforts for analytical validation studies supporting CLIA LDT and IVD approvals.
- Perform statistical analyses such as sample size, power, agreement, precision, and LoD calculations.
- Author documentation of analysis plans, methods, results, and interpretation.
Qualifications:
- Master's or PhD in biostatistics or statistics with relevant experience.
- At least 4 years of practical experience with R, SAS, or JMP.
- Previous diagnostic experience and knowledge of CLSI guidelines.
Knowledge, Skills, and Abilities:
- Expert knowledge of statistical methodology in diagnostic medicine.
- Strong communication skills to explain complex concepts to non-statistical audiences.
- Proven ability to work on cross-functional teams with diverse backgrounds.
Our Opportunity:
- Work at a global leader in cell-free DNA testing dedicated to oncology, women's health, and organ health.
- Collaborate with highly dedicated professionals from world-class institutions.
- Enjoy competitive benefits including medical, dental, vision, 401(k), and parental leave.
Natera
Natera is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. The team consists of highly dedicated professionals from world-class institutions who care deeply for their work and each other.