Floridian Clinical Research offers extensive experience in the following specialties:
Our experienced and dedicated Data Management team works closely with the Sponsors and CROs to provide quality data with minimal queries within the sponsor’s timelines. All study data is completed within 2 weeks of study completion or sooner as per Sponsor’s request. Data queries are resolved within 48 hours.The Data Management team has experience with numerous database tools including:
A clinical trial, or research study, is a carefully supervised study in human volunteers to evaluate the safety and effectiveness of an investigational medication or device. The Food and Drug Administration (FDA) requires that all pharmaceutical companies test their new medications or devices before they are allowed to become available to customers. All prescription medications in use today were first proven to be safe and effective in clinical trials.
Participation is completely voluntary. Participants may withdraw at anytime.
Your safety is our highest priority. The ethical and legal codes that govern medical practice also apply to clinical trials, and most clinical research is federally regulated with built in safeguards to protect participants.
No, there is no cost to the patient to participate in a clinical trial.
By choosing to participate in a Floridian Clinical Research study you are making a contribution to the advancement of medicine and science and making a potential impact on the quality of life for millions of people.
You are also choosing to participate with a research organization whose top priority is your safety, comfort, and well-being.
All of our participants are compensated for their time.
We are currently enrolling volunteers with the following conditions:
Nonalcoholic fatty liver disease (NAFLD)
Nonalcoholic Steatohepatitis (NASH)
Diabetes Mellitus Type II
HIV / AIDS
Chronic Kidney Disease
High Liver Enzymes
See if You Qualify:
Thank you for your interest in studies at Floridian Clinical Research.
This form will allow us to collect information about your health history. Your participation in completing this form is completely voluntary.
Your information will only be seen by researchers at Floridian Clinical Research. The information we collect will be kept private and used only for research studies at Floridian. Your health information will not be shared without your permission or except as required by law. Information collected on this form will be stored in our secured recruitment database. If you agree to being included in the recruitment database, you can request at any time that your name and information be removed.
If you qualify for a study at Floridian Clinical Research, you may be compensated for your time and travel.
By completing the information requested below you are permitting Floridian Clinical Research to retain this information in our files. If you prefer to speak to a screening coordinator in-person, please call us at 305-330-9977 and ask to speak to the screening department.
By choosing to participate in a Floridian Clinical Research study you are making a
contribution to the advancement of medicine and science and making a potential impact on
the quality of life for millions of people.