Get Involved
Become a Volunteer
Volunteers are at the heart of every breakthrough. By participating in a clinical study at VMRC you contribute to the development of new treatments — and receive close medical attention from our research team along the way.
Your information is protected and confidential.
- Reply time ≤ 1 business day
- Miami, Florida
- EN / ES
Why participate?
- Access to investigational therapies before they reach the public
- Close medical attention from board-certified physicians
- Compensation for time and travel (varies by study)
- Bilingual support — English and Spanish
- IRB-approved studies with informed consent
What happens after you send this
The first three steps of the study journey. Nothing is committed until you have read and signed the informed consent.
Coordinator review ≤ 1 business day
A bilingual coordinator confirms we received your form and checks the general criteria against your request.
Eligibility call 15–20 min
A short call to confirm that age, condition, medical history, and previous treatments match the protocol.
Informed consent review 30–60 min
You read the IRB-approved informed consent in your preferred language, with the coordinator alongside you. Ask anything you need.
You can stop at any point
Participation is voluntary. You may withdraw at any time without affecting your routine medical care.
Want a faster answer?
Our bilingual AI concierge can answer your questions and walk you through eligibility in real time.
Talk to AI ConciergeIRB-reviewed studies
Every study at VMRC runs under Institutional Review Board oversight and informed consent.
Your data stays yours
Your information is protected, confidential, and handled under our HIPAA notice.
Bilingual, human team
English or Spanish, from the first call to your last visit — with a team that knows you by name.