Manager, Statistical Programming

Natera

. Lead and oversee statistical programming deliverables, including ADS and TLF, ensuring data integrity and regulatory compliance with ICH, GCP, and FDA 21 CFR Part 11 .

Posted 10/12/2026full-timeRemote • United StatesMid-LevelSenior💰 $132,000 - $165,350 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in statistical programming, particularly in R, with a strong focus on regulatory compliance and data integrity. Capable of leading teams and managing programming deliverables for clinical trials and regulatory submissions.

Highest-signal resume keywords

R ProgrammingStatistical ProgrammingClinical Trial AnalysisRegulatory SubmissionsTeam Management

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Statistical Programming DeliverablesADS and TLF GenerationR Package DevelopmentData IntegrityRegulatory ComplianceProgramming Infrastructure MaintenanceR Shiny Dashboard DevelopmentStatistical Computing Environment MaintenanceAnalysis Dataset GenerationGCP Compliance

Soft Skills

Technical Development SupportCross-Functional Collaboration

Industry Keywords

ICHFDA 21 CFR Part 11510(k)CTA/CDxPMANGSGeneticsOncology Diagnostics

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Lead and oversee statistical programming deliverables, including ADS and TLF, ensuring data integrity and regulatory compliance with ICH, GCP, and FDA 21 CFR Part 11
May manage a team of statistical programmers, supporting their technical and professional development while contributing hands-on to programming work
Act as primary programming lead for regulatory submissions, including 510(k), CTA/CDx, and PMA
Maintain programming infrastructure, including R package development, validation, and maintenance in a controlled environment
Develop R Shiny dashboards supporting 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

Requirements

What you’ll need

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

Benefits

Comp & perks

Comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents
Free testing for employees and immediate families
Fertility care benefits
Pregnancy and baby bonding leave
401k benefits
Commuter benefits
Employee referral program