The opportunity
Natera offers genetic risk assessment and diagnostic tests to patients through medical providers. The Clinical Genomics Engineering organization builds software that supports complex, regulated workflows spanning tertiary analysis workflows including variant interpretation, clinical review, and reporting.
What you'll do
Define and drive multi-year product strategy and roadmap across one or more: RIR components, ensuring alignment to clinical quality, regulatory requirements, and commercial scale objectives
Influence platform-level technical direction in partnership with engineering leadership
Partner closely with software engineering, bioinformatics, clinical domain: experts, quality, regulatory, and other product teams
Translate business, clinical, and operational needs into clear, actionable product requirements
Define and evolve end-to-end user workflows, including UI/UX requirements and supporting backend functionality
Drive cross-team alignment on shared data contracts and workflow standards
What they're looking for
- Mentor and raise the bar for product management within the RIR organization
- Own measurable improvements in clinical workflow efficiency, reliability, and operational scalability
- Establish prioritization frameworks that balance regulatory risk, clinical: impact, technical scalability, and business outcomes across RIR investments.
- Develop and track quantitative metrics related to usability, performance, reliability, and adoption
