Manager of Statistical Programming

United States·San Carlosmid

Other

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Quick Summary

Key Responsibilities

Lead and oversee statistical programming deliverables, including ADS (Analysis Datasets) and TLF (Table, Listings and Figures), ensuring data integrity and regulatory compliance with ICH, GCP,

Requirements Summary

Bachelor’s in Statistics, Mathematics, Computer Science, or a related field. 5+ years of related experience, with at least 3 years of experience in Clinical Trial analysis.

Technical Tools

Other

This is an exciting opportunity to participate in advancing Natera’s oncology product portfolio of cutting-edge diagnostic tests. As Manager of Statistical Programming, you will leverage your strong R programming skills and clinical trials background to contribute to the analysis and reporting of clinical trials supporting multiple regulatory submissions.

Responsibilities

~1 min read

→Lead and oversee statistical programming deliverables, including ADS (Analysis Datasets) and TLF (Table, Listings and Figures), ensuring data integrity and regulatory compliance with ICH, GCP, and FDA 21 CFR Part 11.
→May manage a team of statistical programmers, taking responsibility for their technical and professional development, while contributing hands-on to programming work.
→Act as primary programming lead for regulatory submissions (e.g., 510(k), CTA/CDx, and PMA), ensuring all deliverables meet rigorous global standards.
→Maintain programming infrastructure, including R package development, validation, and maintenance in a controlled environment.
→Develop R Shiny dashboards that support data review, study monitoring, and exploration of analysis results.
→Promote statistical programming development and validation best practices.
→Work cross-functionally with Biostats, Data Management, Clinical Science, and other functions as necessary.

Requirements

~1 min read

Bachelor’s in Statistics, Mathematics, Computer Science, or a related field.
5+ years of related experience, with at least 3 years of experience in Clinical Trial analysis.
At least 3 years of R programming experience, including package development.

Proficient in R programming, including building and maintaining packages.
Experience in analysis dataset and TLF generation.
Prior experience in NGS, genetics, and/or oncology diagnostics preferred.
Experience maintaining statistical computing environments a plus.

What We Offer

~2 min read

This range reflects a good-faith estimate of the base pay we reasonably expect to offer at the time of hire. Final compensation will vary based on experience, qualifications, and internal equity considerations.

This position is also eligible for additional compensation and benefits through Natera’s robust Total Rewards program, including:

✓Annual performance incentive bonus

✓Long-term equity awards

✓Comprehensive health benefits (medical, dental, vision)

✓401(k) with company match

✓Generous paid time off and company holidays

✓Additional wellness and work-life benefits

Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.

The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.