Skip to content
Valencia Medical & Research Center

Get Involved

Become a Volunteer

Take part in a clinical study at VMRC, help advance new treatments, and receive close medical attention from our research team.

Complete pre-screening

Your information is protected and confidential.

  • Reply time ≤ 1 business day
  • Miami, Florida
  • EN / ES

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.

  1. Coordinator review

    A bilingual coordinator confirms we received your form and checks the general criteria against your request.

    ≤ 1 business day

  2. Eligibility call

    A short call to confirm that age, condition, medical history, and previous treatments match the protocol.

    15–20 min

  3. Informed consent review

    You read the IRB-approved informed consent in your preferred language, with the coordinator alongside you. Ask anything you need.

    30–60 min

You can stop at any point

Participation is voluntary. You may withdraw at any time without affecting your routine medical care.

See all eight steps

IRB-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 Notice of Privacy Practices.

Bilingual, human team

English or Spanish, from the first call to your last visit — with a team that knows you by name.