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About Us
Our History
ARA Professionals, LLC is a privately owned clinical research firm specializing in Phase I–IV clinical trials. Our experienced Principal Investigators and dedicated site staff have successfully conducted studies across a wide range of therapeutic areas. We are committed to advancing medical science by partnering with the pharmaceutical industry to support the discovery and development of new medicines and healthcare solutions that improve lives. With a proven track record and a strong foundation in clinical operations, ARA brings deep expertise and reliability to every trial we undertake.
Our Mission
At ARA, we ensure every project receives the same level of focused attention and care. We adhere strictly to agreed-upon budgets and timelines—without ever compromising the quality of our data. Our tailored approach allows us to meet each sponsor’s unique needs with precision, reliability, and a commitment to excellence. sponsor's unique needs are met.
Meet out Investigators
• Jose Luis Garcia, MD – Internal Medicine
• Eduardo Lopez Del Castillo, MD – Family Medicine
• Dean R Heller, MD – Cardiology
• John E Sokolowicz, MD – Cardiology
• Judith E Crowell, MD – Dermatology
• Sergio M Rodriguez, MD – Gastroenterology
• Orlando F Torres, MD – Gastroenterology
• Rafael G Ortiz, MD – Ophthalmology
• Amir Cukierman, OD – Optometry
• Cesar E Ceballos, MD – Orthopedic Surgeon
• Yoave Shimonzvi, MD – Orthopedic Surgeon
• Julio Robla, MD – Orthopedic Surgeon
• Yohandy Fuentes, DPM – Podiatry
• Farhad Abid, MD – Nephrology
• Victor Lopez De Mendoza, MD – Nephrology
• Francisco Pons, MD – Nephrology
• Henry Lujan, MD – Colorectal Surgeon
• Enrique Fraga, MD – Cardiothoracic Surgeon
• Athanasios Tsoukas, MD – Vascular Surgeon
• Roberto Hernando, MD – Psychiatrist / Neurology
• Juan Barrio, MD – Pulmonologist
• Marino E Corniel, ARNP – Sub Investigator
• Judit Alemany, ARNP – Sub Investigator
Volunteer Invitation Box
As a volunteer, you play a vital role in helping find cures for ailments and improving the health of millions worldwide who suffer from various medical conditions. Volunteers in our clinical trials take an active role in their own healthcare. Throughout the study, every volunteer receives exceptional medical care in a comfortable and supportive environment.
All of our studies are conducted in accordance with internationally recognized guidelines, with subject safety as our highest priority. We strictly follow each study protocol, and our principal investigators carefully evaluate every participant. Our team of qualified medical professionals and highly trained investigators is available around the clock to monitor your well-being.
You will undergo regular health checks to ensure your safety and continued good health throughout the trial.
Currently Enrolling Studies
Primary Membranous Nephropathy (PMN)
• Phase: 3
• Age: >18 years
• Study Duration: 13.5 months
• Compensation: $1,600 (includes time and travel)
Self-Reported Drug Users
• Study Duration: 1 visit
• Specimen Collection: Oral fluid
• Compensation: $50
Moderate to Severe Atopic Dermatitis
• Phase: 3 Open-Label
• Age: 12–17 years
• Study Duration: 52 weeks
• Compensation: $100 per visit
Chronic Rhinosinusitis without Nasal Polyps
• Phase: 3
• Duration: 48 weeks
• Compensation: $100 per visit
Chronic Rhinosinusitis with Nasal Polyps
• Phase: 3
• Duration: 52 weeks
• Compensation: $100 per visit
Genotyping Test for Opioid Use Disorder Risk
• Age: ≥18
• Specimen Collection: Buccal (oral) sample
• Study Duration: 1 visit
• Compensation: $100 per visit
Our Services
Site Activation
At ARA, we are committed to accelerating your clinical trials with unmatched efficiency. We guarantee site activation within just a few weeks of site selection, ensuring a swift transition to rapid enrollment and helping you achieve your recruitment goals on time.
Our seamless collaboration with all Central IRBs streamlines regulatory approvals, making the process smooth and efficient. Additionally, our dedicated financial team works diligently to finalize contracts and budgets promptly—typically within weeks of negotiation—so your trial can proceed without delay.
Partner with ARA for a fast, reliable, and efficient path to clinical trial success.
Data Management
At ARA, our dedicated team of specialized professionals focuses exclusively on data management, ensuring the highest quality and accuracy throughout your trial. We complete data entry within 72 hours and resolve queries within five days, keeping your study on schedule.
Our robust data management team is committed to meeting critical timelines and maintaining strict compliance with eCRF guidelines, so you can trust that your data is handled efficiently and in accordance with industry standards.
Partner with ARA for seamless, high-quality data management that supports the success of your clinical trials.
Recruitment
ARA is a leading clinical research site with a proven track record of meeting and exceeding enrollment goals through strategic recruitment and experienced, specialized investigators. Our targeted approach ensures efficient enrollment—even for complex and hard-to-recruit patient populations.
With a research database of over 10,000 subjects and a diverse physician network, ARA provides direct access to a broad patient population. Our site is affiliated with South Florida ENT Associates and Advance Vision Care (AVC), which operates seven locations across South Florida. Additionally, our Medical Director leads Coral Reef Medical Group (CRMG), a private practice with over 30,000 active patients. These affiliations offer unparalleled access to qualified participants across multiple therapeutic areas.
Partner with ARA for streamlined patient enrollment, high-quality data, and seamless trial execution.
