Fewer than 5% of U.S. physicians run clinical trials, and not for lack of patients. Trial IQ works inside your EHR to surface the trials your own patients qualify for, so you can offer research like any other care option.
Illustrative data · not real patient records
Trial IQ handles everything that used to require a research department, so offering a trial takes minutes of your time, not years of build-out.
Full inclusion/exclusion eligibility is computed against live EHR data (labs, biomarkers, medications, treatment history) inside the workflow you already use. No portals, no manual chart review, no guesswork from diagnosis codes.
Today, a patient who wants a trial leaves your practice to get one, and their care often follows. With Trial IQ, the trial comes to you: your patient hears about research from the physician they trust, and treatment stays in your building.
Readiness scoring, sponsor coordination, and the framework for GCP training and regulatory setup: built in. We make sponsors want to invest in you. You bring the clinical judgment.
Per-trial revenue lands on the infrastructure and patient relationships you've already built, with per-patient economics that make research a durable service line — not a side project.
Sponsors and CROs pay for the research. You pay nothing. Trials bring revenue to your practice, and the platform, matching, and readiness support that get you there are free.
Nothing. Sponsors and CROs fund clinical research — that is how trials have always been financed. Trial IQ is paid on the sponsor side, so matching, onboarding, and readiness support come at no cost to your practice, and per-trial revenue flows to you.
Minutes, not hours. Matching runs in the background against your EHR, and a flagged patient shows up in the workflow you already use. Raising a trial with a patient takes about as long as discussing any other treatment option. The sponsor coordination, regulatory setup, and training around it are what we absorb.
No. Most physicians we work with have never run a trial. Readiness scoring shows exactly what is missing, and we support GCP training, regulatory setup, and sponsor coordination end to end. If research grows into a real service line, hiring a coordinator becomes a revenue decision, not a prerequisite.
No. That is the point. Traditional recruitment pulls your patient to a distant site, and their care often follows. With Trial IQ the trial comes to your practice: you remain the treating physician, and care stays in your building.
Clinical data under a BAA, scoped to what matching requires. Matched patients are identified to you and your staff alone, and you decide how and when to raise a trial with each of them. No patient information reaches a sponsor before the patient says yes, through you.
Every trial runs under the sponsor's protocol, with investigator responsibilities defined up front and covered in onboarding. Industry studies carry sponsor-side insurance and indemnification, and you see those exact terms before accepting any protocol. You can decline any trial, for any reason.
You can step back at any time. Matching is informational until you accept a protocol. Nothing obligates your practice to take any trial, and there is no penalty for saying no to all of them.
Still have questions? Reach out to us here.
Tell us a little about your practice and we'll show you the enrolling trials your patient panel already matches — before you commit to anything.