Clariva Medical is a nationally focused research coordination service dedicated to connecting individuals with clinical study opportunities — with transparency, respect, and clear communication at every stage.
At Clariva Medical, we believe that clinical research advances only when participants are treated with the care and respect they deserve. Our role is to serve as a trusted bridge between individuals interested in research participation and the investigators and institutions conducting studies across the country.
We are not a hospital, clinic, or medical practice. We do not prescribe treatments, diagnose conditions, or provide medical advice. What we do is make the path to participation clear, straightforward, and supported at every step.
Clariva Medical operates as a research support and routing service. When you submit your information through our platform, our coordination team reviews your responses and works to identify whether any active studies in our network may be a potential match based on your eligibility criteria.
If a match is identified, we assist with scheduling initial screening conversations with licensed study teams. From that point, all medical and eligibility decisions are made by qualified investigators — not by us.
With your consent, we stay in touch through appointment reminders, status updates, and study notifications so you're always informed without being overwhelmed.
We do not sell, rent, or share your personal information with third-party marketers or advertisers. Your data is used only to coordinate your inquiry and communicate with you as you've requested. For full details, see our Privacy Policy.
We do not provide medical opinions, and we never pressure anyone to participate in or continue a study. Participation is always entirely voluntary, and you may withdraw at any time without consequence.
Clariva Medical operates across all 50 states, working with a broad network of research institutions, investigative sites, and study sponsors to maintain access to a diverse range of active clinical trials. Whether you're in a major metropolitan area or a smaller community, we work to find study opportunities that fit your location and circumstances.
Every study within our network operates under the oversight of an Institutional Review Board (IRB) and follows federally mandated protocols for clinical research. Before enrolling in any study, participants receive a full informed consent process conducted by the study team — explaining risks, benefits, procedures, and your rights as a volunteer.
You can withdraw from any study at any time, for any reason, with no impact on your future healthcare or standing with Clariva Medical.
Submitting your information is free, voluntary, and takes only minutes. Let us do the coordination work while you focus on what matters most.