Remote opportunity at
NateraManager of Statistical Programming
Natera is seeking a Manager of Statistical Programming to join its team on a remote basis within the USA. In this position, the professional will advance…
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About This Role
Natera is seeking a Manager of Statistical Programming to join its team on a remote basis within the USA. In this position, the professional will advance the company's oncology diagnostic portfolio by supporting clinical trials and regulatory filings. Natera operates as a global leader in cell-free DNA testing, focusing on oncology, women’s health, and organ health with the goal of making personalized genetic testing standard practice. This opportunity is well-suited…
Job Description
Natera is seeking a Manager of Statistical Programming to join its team on a remote basis within the USA. In this position, the professional will advance the company's oncology diagnostic portfolio by supporting clinical trials and regulatory filings. Natera operates as a global leader in cell-free DNA testing, focusing on oncology, women’s health, and organ health with the goal of making personalized genetic testing standard practice.
This opportunity is well-suited for an experienced statistical programmer with a clinical trials background and strong R capabilities who can deliver data integrity and regulatory compliance. The person in this role will oversee programming deliverables, potentially manage a team, and maintain statistical computing environments. Day-to-day work involves creating analysis datasets, generating tables, listings, and figures, building R Shiny dashboards, and collaborating cross-functionally with groups such as Biostats and Data Management.
Responsibilities
- Manage and direct statistical programming output, encompassing analysis datasets along with tables, listings, and figures
- Ensure compliance with ICH, GCP, and FDA 21 CFR Part 11 standards for data integrity
- Potentially supervise a team of statistical programmers while handling technical and professional growth alongside hands-on tasks
- Act as the main programming contact for regulatory submissions including 510(k), CTA/CDx, and PMA
- Oversee, build, and validate R programming infrastructure and packages within a controlled setting
- Create R Shiny dashboards to aid in data review, study oversight, and analysis exploration
- Partner cross-functionally with Biostats, Clinical Science, and Data Management teams
Requirements
- At least 5 years of related professional experience
- Minimum of 3 years of experience working in clinical trial analysis
- At least 3 years of R programming experience, covering package development
- Background in generating analysis datasets and table, listing, and figure outputs
Qualifications
- Bachelor degree in Statistics, Mathematics, Computer Science, or a related discipline
- Prior familiarity with next-generation sequencing, genetics, or oncology diagnostics
- Experience with the maintenance of statistical computing environments
Core Skills
Benefits
- Medical, dental, vision, life, and disability insurance plans for eligible employees and dependents
- Complimentary testing and fertility care benefits for employees and immediate families
- Pregnancy and baby bonding leave
- 401(k) retirement benefits
- Commuter benefits
- Employee referral program
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
Is this position remote?
Yes, the posting lists the remote status as Remote USA.
What is the salary range for this role?
The remote USA pay range is $132,000 to $165,350 USD, with actual compensation varying based on skills, experience, certifications, and location.
What education is required?
Candidates need a bachelor degree in Statistics, Mathematics, Computer Science, or a related field.
What experience is necessary?
Applicants must have at least five years of related experience, with a minimum of three years in clinical trial analysis and three years of R programming.
Sample Interview Questions
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