South Miami, Florida · Phase II–IV clinical trials

Better medicine. Better lives.

USPA Advance Concept Medical Research Group turns research into real treatment. We run Phase II–IV trials in South Miami with a multidisciplinary network of specialists, and we are recruiting volunteers now.

Internal Medicine · Family Practice · Gastroenterology
Psychiatry · PMHNP-BC · Cardiology
6356 Manor Ln, Suite 102, South Miami, FL 33143

A study coordinator recording a participant's vitals during a clinical trial visit
Study visit · USPA research site
20+ Years of combined clinical research experience
35,000+ Prescreened subjects in our database
II–IV Trial phases conducted on site
15MIN From Miami International Airport, next to South Miami Baptist Hospital

Who we are

Passionate about improving medicine.

Since June 18, 2020, USPA has been dedicated to advancing medical research. Our team brings over 20 years of combined clinical research experience across South Florida and international sites, and specializes in Phase II–IV trials supported by a multidisciplinary network of physicians and nurse practitioners.

We have run studies in NASH/MASH, Crohn’s disease, ulcerative colitis, gastroparesis and COPD, among others. Our work spans respiratory, gastroenterology, cardiology, psychiatry and dermatology, helping drive innovation and improve patient outcomes.

Backed by a database of more than 35,000 prescreened subjects and a location 15 minutes from Miami International Airport, adjacent to South Miami Baptist Hospital, our key research partner, we offer recruitment reach and operational efficiency that few sites in the region can match.

  • Internal Medicine
  • Family Practice
  • Gastroenterology
  • Psychiatry
  • PMHNP-BC
  • Cardiology

Therapeutic areas

What we study.

Our network of specialists lets us run trials across eight therapeutic areas, from central nervous system and infectious disease to dermatology and gastroenterology.

AI

Autoimmune

Autoimmune programs run across the areas below, including Graves' disease, Hashimoto's thyroiditis, multiple sclerosis, psoriasis and celiac disease.

CNS

Central nervous system

  • Alzheimer's disease
  • Parkinson's disease
  • ADHD
  • ADD
ID

Infectious disease

  • HIV
  • COVID-19
  • RSV
  • Seasonal influenza
ENDO

Endocrine

  • Type 1 diabetes
  • Graves' disease
  • Hashimoto's thyroiditis
  • Addison's disease
NEURO

Neurological

  • Multiple sclerosis
  • Myasthenia gravis
  • Guillain-Barré syndrome
DERM

Dermatological

  • Psoriasis
  • Eczema
  • Vitiligo
  • Discoid lupus
GI

Gastrointestinal

  • Crohn's disease
  • Ulcerative colitis
  • Celiac disease
  • Gastroparesis
  • NASH/MASH
RESP

Respiratory

  • COPD

Do not see your condition? Our recruitment database is matched against every new protocol we take on. Tell us what you are living with and we will contact you when a study fits.

Join a study

Why get involved

Access tomorrow's medicine today.

Join a clinical trial and gain access to innovative treatments while helping us discover the medications of tomorrow. Together we are shaping the future of medicine.

01

Receive compensation

Many clinical trials offer payment or reimbursement for your time, travel and participation.

02

Health monitoring and support

Trials include regular check-ups, tests and personalized monitoring from medical professionals.

03

Access to cutting-edge treatment

Volunteers may gain early access to innovative therapies that are not yet widely available.

04

Empowerment and giving back

You play an active role in advancing science and helping future patients, making a real difference.

How a study works

Four stages, from protocol to publication.

Stage 01

Planning and study design

Researchers define the goal of the study, create the protocol, obtain FDA and IRB approvals, and recruit eligible participants.

Stage 02

Enrollment and screening

Volunteers are evaluated through interviews, medical history and lab tests to confirm they meet all study criteria.

Stage 03

Treatment and data collection

Participants receive the investigational drug or placebo while researchers monitor outcomes, safety and side effects.

Stage 04

Analysis and reporting

Data is analyzed to determine safety and effectiveness, then submitted to regulatory agencies and shared with the scientific community.

What to expect when you volunteer

  • Quick screening process
  • Access to innovative treatment
  • Comprehensive health monitoring
  • Personalized care and support
  • Compensation for time and travel
  • Safe, regulated environments

Our partners

Reliable data for safer innovation.

We partner with major brands across the country to produce reliable clinical data that drives smarter, safer healthcare innovation. Our site sits adjacent to South Miami Baptist Hospital, our key research partner, and 15 minutes from Miami International Airport.

A nurse and a participant smiling together during a study visit

What participants tell us

Participants report a greater sense of hope for a better quality of life.

Many appreciate the opportunity to help others by contributing to the development of new treatments for diseases, and they often feel well supported throughout the care and treatments provided.

Frequently asked questions

Before you volunteer.

What is a clinical trial?

A clinical trial is a research study that tests new treatments, medications or procedures to see if they are safe and effective.

Why should I participate in a clinical trial?

Participation allows you to access cutting-edge treatments, receive expert medical care, and contribute to advancing medicine for others.

Is it safe to participate?

Yes. Clinical trials follow strict safety protocols, are closely monitored by medical professionals, and are approved by regulatory boards to protect participants.

Will I be compensated for participating?

Many clinical trials offer compensation or reimbursement for your time, travel and other related expenses.

How long will the study last?

The duration varies depending on the trial, ranging from a few weeks to several months or longer.

What will happen during the trial?

Participants may undergo health screenings, regular check-ups, lab tests, and receive treatments or medications according to the study plan.

Can I leave the study if I change my mind?

Yes. Participation is voluntary, and you can withdraw at any time without affecting your regular medical care.

Will my personal information be protected?

Absolutely. Clinical trials follow strict privacy laws, and your personal and medical information is kept confidential.

Join a study

Ready to participate?

Send us a message or give us a call. If you are a current patient and would like to book an appointment, or you would like to apply to become a patient, our team will get back to you within 24 hours.

If you have a life threatening emergency, call 911.

    Request a screening

    Your information is kept confidential and used only to check your eligibility for current and upcoming studies.