Senior Ux Researcher, Human Care

Oura Oura · Consumer · San Francisco, CA +1 · Design

Senior UX Researcher for Oura's Human Care mission, focusing on products at the intersection of consumer experience and healthcare. Responsibilities include leading user research, understanding clinical and regulatory context (FDA, HIPAA), and developing frameworks for surfacing clinical data to consumers. Requires 5+ years of UX research experience in healthcare/digital health and experience with regulated environments.

What you'd actually do

  1. Lead user research for the software team connecting members to healthcare partners. Plan, conduct, and analyze a range of user research studies, including ethnographic studies, contextual inquiries, user interviews, surveys, and diary studies to gather both qualitative and quantitative data.
  2. Bring clinical and regulatory context into product decisions — understanding how FDA-regulated features, HIPAA consent flows, and EHR integrations shape what's possible and what's appropriate for members.
  3. Develop research-backed frameworks for how Oura surfaces clinical-grade data (biomarkers, lab results, risk signals) to consumer audiences in a way that's clear, actionable, and emotionally resonant — not alarming.
  4. Partner with the clinical and health science teams to ensure research bridges behavioral and physiological insight — understanding not just what users do but what health context drives those behaviors.
  5. Build and maintain a longitudinal view of our members from the lens of connected care— their motivations, anxieties, health literacy, and relationship with clinical care — that informs roadmap prioritization.

Skills

Required

  • 5+ years of professional UX research experience
  • Meaningful work at the intersection of consumer product and healthcare, digital health, or clinical technology
  • Demonstrated ability to research complex, high-stakes experiences — medical devices, clinical software, diagnostic tools, telehealth, or patient-facing health apps
  • Deep understanding of health literacy variation across populations
  • Experience navigating regulated or compliance-sensitive environments (HIPAA, FDA, IRB)
  • Strong point of view on how to make clinical data legible and meaningful to non-clinical audiences
  • Proven experience working in cross-functional teams including PMs, clinicians, designers, data scientists, and commercial teams
  • Ability to operate independently across multiple concurrent workstreams
  • Prioritize ruthlessly
  • Build a research program that is respected

Nice to have

  • Experience researching connected care or care coordination products
  • Familiarity with metabolic health, GLP-1 medications, or cardiometabolic care pathways
  • Prior work with B2B healthcare products

What the JD emphasized

  • clinical and regulatory context
  • FDA-regulated features
  • HIPAA consent flows
  • clinical-grade data
  • regulated or compliance-sensitive environments
  • HIPAA
  • FDA
  • IRB