Clinical Research Site · West Palm Beach, FL

An axiom needs no proof. Good evidence does.

Axiom Research Group is an independent clinical research site conducting Good Clinical Practice (GCP)-aligned studies in Palm Beach County — turning rigorous protocols into real answers for patients, physicians, and sponsors.

1Dedicated research site
MDPrincipal Investigator: Horacio Valladares
+1Clinical partnership: Montesol Medical Centers
axiom

/ˈak·see·uhm/

noun
  1. A statement so clear and evident that it is accepted without proof.
  2. A starting point upon which rigorous knowledge is built.
Who we are

First and foremost, a clinical research site.

Axiom Research Group is an independent clinical research site in West Palm Beach, Florida. We design and conduct studies with the same rigor our name suggests: transparent methods, careful documentation, and results that stand on their own. For participant recruitment, we maintain a clinical partnership with Montesol Medical Centers, which serves an established patient community in the neighborhood.

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Active protocols

Studies open for enrollment

Every protocol is conducted under Institutional Review Board (IRB) oversight and with informed consent. These are the studies currently running at our site.

Professional preparing samples in a clinical research laboratory
Our site

What sets us apart

We are not a primary care clinic: we are a site dedicated exclusively to clinical research. Every visit, every sample, and every data point is collected following the study protocol and Good Clinical Practice.

Our team combines medical experience with research discipline: close follow-up of every participant, meticulous documentation, and clear communication with sponsors and monitors.

Clinical recruitment partnership

Axiom + Montesol Medical Centers

Axiom Research Group
MonteSol Medical Centers

We work alongside Montesol Medical Centers, a group of medical centers with an established patient community in West Palm Beach. This partnership lets us identify potential participants responsibly — always with the patient’s authorization and under ethical oversight.

About the partnership

Healthcare professional checking the blood pressure of a smiling patient

Why participate in a study?

Participation is voluntary and always begins with an informed consent process.

No cost

Study assessments and study medication are provided at no cost to the participant. Some studies compensate for time and travel.

Close follow-up

Scheduled visits, periodic assessments, and direct access to the study team throughout your participation.

Contribute

Your participation helps answer real medical questions and develop treatments for future generations.

Participant benefit

Free, unlimited transportation

No way to get to the site? We will take you. We pick up participants who need it and take them back home for every study visit — at no cost and with no limit on trips.

Compliance and ethics

Participant protection comes first

HIPAAYour medical information is protected under federal health privacy law.
GCPWe conduct every study according to international Good Clinical Practice.
IRBAn independent ethics board reviews and oversees every protocol.

Ready to take the first step?

Tell us about yourself and we will help you find out whether you qualify for one of our active studies. No obligation.

Contact us
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