Clinical Research Associates of South Florida (CRAOSF) is a multi-specialty research facility proficient in Phase II-IV clinical trials in South Florida. Our diversified and extensive industry experience enables us to offer our sponsors and patients a quality research site with a trained and experienced clinical research team. CRAOSF is commited to actively search for new ways to improve the health of our patients and quality of life.

We are centrally located in the city of Miami, 9 miles from Miami International Airport and 2 miles from a major hospital. 

Our 2,200 sq. ft. facility is temperature controlled and fully equipped:

• 3 patient exam rooms

• CLIA Certified Clinical Laboratory

• Large conference room

• Dedicated coordinator room

• Private office specifically designated for pharmaceutical company sponsors and/or use for monitors

• Waiting room with TV for subjects with comfortable seating

• Ample storage space for confidential patient records and sensitive clinical trial information

• All study drug is kept in a double lock secure medication room

• Storage is locked at all times and is only accessible to assigned clinical personnel by individual key card access. Limited access is strictly enforced.

• Refrigerators, -20 & -80°C Freezers

• 24/7 Electronic Temperature Monitoring System with Min and Max temperature recording

• Refrigerated and standard centrifuges

• ECG machines

• Backup generator in case of power failure

• High speed wireless internet access throughout

• Kitchen/Dining Room
• Private area for ICF process and/or Subject questionnaires
• Fully equipted laboratory
• Crash cart with defibrillator

CRAOSF Staff has over 15 year experience.

• Board Certified Physicians
• ARNP/DNP/PhD
• Director of Research
• Principal Investigators
• Clinical Research Coordinators
• Medical Assistant Quality Assurance
• Professional Bilingual Friendly staff
• Established relationships with specialists

All Staff are Certified & Trained in:

•  
• GCP Certified
• IATA Certified
• CPR/PBLS/ACLS Certified
• Laboratory Procedures
• Trained in IVRS, EDC, and Central Laboratory
• Maintenance of Investigator Study File and Source Documents
• Completion of CRF and Study Documents