FOR PATIENTS

CLINICAL TRIALS

Floridian Clinical Research offers extensive experience in the following specialties:

  • Asthma/COPD/Allergy
  • Atopic Dermatitis
  • Cardiovascular disease
  • Crohn’s Disease
  • Dermatology
  • Endocrinology
  • Gastroenterology
  • Gynecology
  • Neurology
  • Pain Management
  • Pharmacology/Toxicology
  • Pruritus in Renal Patients
  • Psoriasis
  • Psychiatry
  • Rheumatology
  • Sexual Dysfunction
  • Urology/Nephrology
  • Women’s Health

LABORATORY SERVICES

Floridian Clinical Research partners with local and central laboratories to service all laboratory needs for our clinical trials. These laboratories are fully qualified with CLIA and state licensure. Our on-site, state-of-the-art lab facility, offers a full suite of laboratory services from pick-up to electronic reporting. The lab is furnished with the most advanced equipment and instruments, guaranteeing the highest level of accuracy and reliability. We guarantee same-day turnaround.

A certified Clinical Lab Director supervises all procedures and a third party survey and audit process provides independent oversight, quality control, and adherence to the strictest standards of safety and compliance.

Our quality process includes:

  • Full Certificate of Registration for CLIA High Complexity testing
  • State-of-the-art calibrated equipment to ensure accurate results
  • Experienced onsite staff
  • Onsite phlebotomist
  • Open 7 days a week
  • Specimen pick up 7 days a week
  • Electronic reporting of test results
  • Guaranteed same-day turnaround

DIAGNOSTIC SERVICES

Floridian Clinical Research provides internal and external diagnostic services. These services include:

  • Asthma/COPD/Allergy
  • Blood Gas Analyzer
  • Spirometry/Pulmonary Function Test
  • Pulse Oximetry
  • VO2 Max/Ergometry
  • Multiple/Serial ECGs
  • Holter Monitoring
  • Telemetry
  • Ambulatory Blood Pressure Machine
  • Glucose Monitoring
  • X-rays
  • CT Scans
  • MRI
  • DEXA Scan
  • Mammography
  • Ultrasounds
  • Biopsy
  • Meal Tolerance Tests
  • NCV/EMG (Nerve Conduction Velocity/Electromyography)
  • Urine Collections
  • Urodynamics

DATA MANAGEMENT

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:

  • Datatrack
  • Inform
  • Rave
  • Immedidata
  • Timaeus
  • Viotec
  • RDC
  • Eraphase
  • Egate
  • Medrio

MEDICAL & PHARMACY SERVICES

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:

  • 1 Full-time, on-site Principal Investigator
  • 1 Full-time, on-site Sub Investigator
  • Multi-Specialty on-site Investigators and Sub Investigators
  • 24/7 coverage by licensed medical personnel
  • All medical staff certified in BLS and ACLS
  • Medical staff experienced in all levels of acute care
  • Pharmacy Director
  • DEA license schedule II-V
  • Secure, limited-access pharmacy
  • Full range of refrigeration capabilities
  • DicksonOne temperature and humidity monitoring 24/7
  • Laminar flow hood
  • Experienced with IV, IM, SQ, Oral, Topical, Transdermal and Sublingual administration

Frequently Asked Questions

What is a clinical trial?

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.

Can I leave the study once I join?

Participation is completely voluntary. Participants may withdraw at anytime.

Is there any cost to participate?

No, there is no cost to the patient to participate in a clinical trial.

Are clinical trials safe?

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.

Current Studies

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:

Low Testosterone
Diabetes Mellitus Type II
AIDS (HIV)
Chronic Kidney Disease
High Triglycerides
High Cholesterol
Healthy Volunteers

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.