What We Screen For Before Placement
- Production healthcare UX research experience
- Clinician research access — ability to recruit clinicians for studies
- IRB and PHI-handling fluency
- AI trust UX or accessibility specialization
Healthcare UX is not consumer UX. A clinician using your software has 6 minutes per patient. A patient using your portal may be in pain, in distress, or in the middle of a diagnosis they do not understand. An AI feature that suggests a treatment can be ignored, accepted, or accepted-with-override — and the override pattern matters more than the model accuracy. Building healthcare software without specialized UX research is shipping blind.
Taction Software’s healthcare UX researchers have run clinician workflow studies inside hospitals, AI-trust evaluations on clinical copilots, patient-portal usability studies across language and accessibility constraints, and field research on RPM adherence. Every researcher has worked under a BAA. Engagements start at $8,000 per researcher per month with a 14-day onboarding window and a Business Associate Agreement signed before any PHI touches our systems.
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For background, see our coverage of healthcare AI clinician trust design and our work on ambient documentation for a 12-clinic group.
$8,000 per researcher per month with a 3-month minimum.
$24,000 to $40,000 per month for a pod of 3 to 5 researchers covering clinician, patient, and AI-trust streams.
For estimates, use the healthcare AI cost calculator.
$8,000 per researcher per month with a 3-month minimum.
14 days from discovery to researcher-on-team.
Yes. Clinician recruitment is part of the research capability, including time-of-day, specialty-specific, and EHR-vendor-specific recruitment.
Yes. We handle IRB review for studies that require it, working with your institution’s IRB or a commercial IRB depending on scope.
Yes. Clinician override behavior, citation grounding, and AI confidence calibration are core specializations. See our healthcare AI clinician trust design page.
Yes. Human factors engineering for SaMD submissions is supported, typically paired with our FDA SaMD engineers.
Yes. Every engagement begins with a BAA.
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Our expert reaches out shortly after receiving your request and analyzing your requirements.
If needed, we sign an NDA to protect your privacy.
We request additional information to better understand and analyze your project.
We schedule a call to discuss your project, goals. and priorities, and provide preliminary feedback.
If you're satisfied, we finalize the agreement and start your project.