We are dedicated to advancing medicine through safe, ethical, and innovative clinical trials. Founded and led by experienced physicians, our site partners with global pharmaceutical and biotechnology companies to bring breakthrough treatments closer to the patients who need them most.
We combine clinical expertise with compassionate care, ensuring that every participant is respected, informed, and supported throughout their research journey.
Our Mision
To improve health outcomes by conducting high-quality clinical research that meets the highest standards of scientific integrity, patient safety and regulatory compliance.
Our Vision
To be a trusted leader in clinical research, known for our excellence in data quality, participant experience, and collaboration with sponsors and CRTOs.
Our Values
Integrity: We uphold transparency and ethical conduct in every study.
Excellence: We strive for precision, efficiency, and reliability in our research process.
Compassion: We care deeply for our participants and their contribution to science.
Innovation: We embrace new technologies and methods that improve outcomes.
Our Facility
Our modern research center in Miami, Florida is fully equipped for Phase II-IV clinical trials, including:
-Dedicated exam and infusion rooms
-On-site laboratory with sample processing capabilities
-Secure data management systems
-Comfortable participant waiting areas
-Emergency equipment and physician coverage.
Gallery coming soon
Our Team
Led by Dr Maria Curbelo Calleiro, Principal Investigator, our multidisciplinary team includes sub-investigator, Crosleivis Rodriguez, APRN, study coordinators, nurses, and regulatory specialists all trained in Good Clinical Practice (GCP) and committed to research excellence.
Why Participate in a Clinical Study?
Clinical Research helps discover better ways to prevent, diagnose and treat medical conditions. By joining a study at MDC Clinical Research, you play an important role in advancing science and you may gain early access to new treatments under expert medical supervision.
What to Expect
1-Screening: You will first complete a screening visit to determine if you meet the study requirements.
2-Enrollment: If eligible, you will review and sign an informed consent from before any stuDy procedures begin.
3-Study Visits: You will attend scheduled visits for exams, lab test, or questionnaires. Our team will monitor your safety and well-being throughout.
4-Follow-up: After your participation ends, we may contact you for a short follow-up to ensure your continued health and collect final data.
Your Safety Matters
All Studies are reviewed and approved by an Institutional Review Board (IRB) tp protect your rights and safety. You may withdraw from a study at any time, for any reason without affecting your medical care.
Benefits of participation
Access to innovative medical treatments
Comprehensive health assessments at no cost
Compensation for time and travel(varies by study)
The opportunity to help others through science.
Get Involved
Interested in joining a study or partnering with us?
Fill out our from or call us at:
305-425-1343 to learn how you can take part in the future of medicine.