Own the product lifecycle for RNA-based diagnostics, driving user discovery, defining product requirements, and leading go-to-market strategies with various teams.
Viome is a pioneering health technology company that leverages artificial intelligence and RNA-based molecular diagnostics to transform healthcare through precision medicine. Our Diagnostic Division (ViomeDx) empowers healthcare providers with advanced molecular insights that enable early detection, personalized treatment, and improved patient outcomes.
Built on a foundation of over 600,000 analyzed samples and 52 petabytes of data, Viome's proprietary AI platform delivers clinically validated, RNA-based diagnostic tests that help providers detect disease early, treat precisely, and prevent illness before it manifests. We serve concierge medicine practices, functional medicine providers, and direct-pay specialists who are committed to delivering personalized, preventive care.
Our mission is to create a healthcare system where providers have access to the most advanced molecular diagnostics, enabling them to build stronger patient relationships while delivering measurably better health outcomes.
About the role: Own the end-to-end product lifecycle for RNA-based diagnostic offerings—from problem discovery to launch/scale—working cross-functionally with Clinical, Lab Ops, Engineering/AI, Regulatory, and Commercial to deliver clinically valuable, provider-loved solutions.
What you’ll do
- Drive discovery (user interviews, workflow mapping, JTBD, requirement docs, PRDs, acceptance criteria).
- Translate clinical utility and regulatory constraints into clear product requirements and roadmap prioritization.
- Partner with Lab Ops/Engineering to scope, deliver, and iterate on assays, reports, and provider portals.
- Define and monitor success metrics (adoption, turnaround time, quality, NPS/CNPS, revenue/margin) and run experiments to improve them.
- Lead go-to-market with Marketing and Sales; craft positioning, pricing hypotheses, and enablement.
- Ensure compliant releases (documentation, labeling, intended use claims) in partnership with Regulatory/Quality.
- Capture field feedback and competitive intelligence; feed into roadmap and build/buy/partner decisions.
What you bring
- 4–8+ years product management in diagnostics, digital health, or clinician-facing SaaS (ideally with LDTs/molecular diagnostics).
- Strong system thinking—comfortable spanning UX, science, data/AI, and lab constraints.
- Excellent PRD writing, prioritization, and stakeholder facilitation.
- Familiarity with regulated environments and design controls; data-informed decision-making.
- Bonus: experience with value-based care economics, HL7/FHIR integrations, or provider portal/reporting UX.
- Advanced science degree; prior founder/startup experience; experience partnering with MSL/Medical Affairs.
Nice to have:
We are an equal opportunity employer and do not discriminate based on race, color, religion, sex, national origin, age, disability, or any other legally protected status. We value diversity, equity, and inclusion, and are committed to creating a workplace that reflects these values.
Top Skills
AI
Fhir
Hl7
Prds
Rna-Based Diagnostics
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