POSITION SUMMARY:
This is an exciting opportunity to participate in advancing Natera’s oncology product portfolio of cutting-edge diagnostic tests. As a Lead Statistical Programmer, 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.
PRIMARY RESPONSIBILITIES:
- Lead programmer for one or more clinical validation studies supporting in vitro diagnostic submissions (e.g., IVDR, 510(k), CTA/CDx/PMA, etc.) including dataset and TFL generation.
- Perform programming validation and maintain documentation as needed.
- Lead development of programming infrastructure, including R package development and
- Contribute to development of junior team members.
QUALIFICATIONS:
- Bachelor’s in statistics, mathematics, computer science, or related field.
- 5+ years related experience with at least 3 years experience in Clinical Trial analysis.
- At least 3 years R programming experience, including package development.
KNOWLEDGE, SKILLS, AND ABILITIES:
- Proficient in R programming including building and maintaining packages.
- Experience in analysis dataset and TFL generation.
- Prior experience in NGS, genetics, and/or oncology diagnostics preferred.
- Experience maintaining statistical computing environments a plus.