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Patient Recruitment

Find a clinical study designed for you.

Explore available studies in Miami and learn how to take part.

Your information is protected and confidential.

Track record

30 clinical studies conducted at VMRC

Pharmaceutical sponsors, biotech companies and academic research networks have run their protocols here — from Phase I to Phase III, in adults, adolescents and young children. Each registered study links to its public record.

Sponsors
17
Pediatric studies
10
Phases conducted
Phases 1 to 3

Sponsors with studies at VMRC

  • AbbVie (6 studies)
  • Ardelyx (4 studies)
  • Areteia Therapeutics (2 studies)
  • AstraZeneca (2 studies)
  • Duke University (NIH RECOVER) (2 studies)
  • Iterum Therapeutics (2 studies)
  • Landos Biopharma (2 studies)
  • Atea Pharmaceuticals (1 study)
  • Chiesi (1 study)
  • Cue Health (1 study)
  • Dermtreat (1 study)
  • Guardant Health (1 study)
  • Ironwood Pharmaceuticals (1 study)
  • Sanofi (1 study)
  • Shionogi (1 study)
  • Sun Pharma (1 study)
  • Uniquity One (1 study)

Study register

30 studies shown

Phase, ages and start year come from each study's public record on ClinicalTrials.gov. Status refers to VMRC's participation as a site.

How we support you throughout the study.

How participation works

A simple, supported process.

Online · about 5 minutes

Illustrative images.

Before you decide

What to know
before taking part.

  • What is a clinical study?

    A research study that evaluates a treatment under a written protocol. Every protocol is reviewed and approved by an independent ethics board (IRB) before a single participant is enrolled, and the study team follows it visit by visit.

  • Does taking part cost me anything?

    Study visits and study procedures are provided at no cost to you, and no insurance is required to participate. What each study covers, including the investigational medication, is written in its consent form, which you review before agreeing to anything.

  • Who oversees my safety?

    A licensed physician serves as principal investigator and is responsible for your care throughout the study. An independent IRB reviews the protocol before it starts and continues to oversee it, and every visit is documented under the supervision of the study's principal investigator.

  • Will I be paid?

    Studies that offer compensation pay for your time and travel, not for taking a medication. The exact amount and schedule are written in the consent form for that specific study, and you review it before agreeing to anything.

  • Can I leave once I have started?

    Yes, at any time and for any reason. Participation is voluntary from the first visit to the last; withdrawing does not affect your regular medical care and you do not have to explain your decision.

  • What happens to my personal information?

    Your records are kept confidential under Florida law and the study's consent form. Data shared with a study sponsor is coded, and your name is not used in any published result.

Still deciding?Talk it through with our team

Why people trust us

Three promises behind every study.

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.

Not sure where to start

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finding a study?

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