Head of Statistical Programming – Oncology Trials

Natera

San Carlos (CA)

Sur place

USD 145 000 - 182 000

Plein temps

Il y a 3 jours
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Avantages offerts par ce poste

Annual incentive bonus
Long-term equity awards
401(k) with company match
Generous paid time off
Wellness benefits

Résumé du poste

Natera is seeking a Manager of Statistical Programming to lead ADS and TLF, oversee regulatory submissions, and build R packages and Shiny dashboards in support of oncology diagnostics.

The role combines strategic leadership with hands-on programming in a fast-paced, cross-functional environment, offering growth opportunities, competitive benefits, and the chance to influence data-driven decisions across multiple trials.

Qualifications

  • Bachelor’s degree in statistics, mathematics, computer science, or related field.
  • 5+ years of related experience, with at least 3 years in clinical trial analysis.
  • At least 3 years of R programming experience, including package development.

Responsabilités

  • Lead and oversee statistical programming deliverables, including ADS and TLF, ensuring data integrity and regulatory compliance.
  • May manage a team of statistical programmers and contribute hands-on to programming work.
  • Lead regulatory submissions (e.g., 510(k), CTA/CDx, PMA) and maintain rigorous global standards.
  • Develop R packages and Shiny dashboards to support data review and study monitoring.
  • Promote best practices in statistical programming development and validation.
  • Collaborate cross-functionally with Biostats, Data Management, and Clinical Science.

Connaissances

R programming
Clinical trial analysis
Team leadership

Formation

Bachelor’s in Statistics, Mathematics, Computer Science, or related field

Description du poste

Natera is seeking a Manager of Statistical Programming to lead ADS and TLF, oversee regulatory submissions, and build R packages and Shiny dashboards in support of oncology diagnostics.

The role combines strategic leadership with hands-on programming in a fast-paced, cross-functional environment, offering growth opportunities, competitive benefits, and the chance to influence data-driven decisions across multiple trials.

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