Ocean Blue Medical Research Center is a multi-specialty clinical research center who conducts clinical trials from Phase I to Phase IV. These studies involve, among many other, therapeutic areas such as: Neurology, Psychiatry, Internal Medicine, Dermatology, Endocrinology, Infectious disease, Rheumatology and Women's health.
Provide our sponsors with competent and professional care to develop clinical research with excellence. Our core is to deliver clinical research data on a timely, accurate and efficient manner to comply with protocol adherence and guidelines.
We strive in becoming a highly recognized clinical research center and improve people's health through the conduction of studies in accordance to the highest standard of excellence for our sponsors and CROs.
Our principals and investigator have more than 40 years of combined experience working specifically in the health care area as well as realizing clinical trials, either for pharmaceuticals, cosmetics or new technological advances and its direct incidence in human health.
Our mission and experience combined with a great location, proper facility and a great team of specialists and superb healthcare professionals, have put Ocean Blue Medical Research Center at the top of all other research centers across South Florida.
Ocean Blue Medical Research Center has demonstrated dedication to protect the safety, ethical concerns and rights of our volunteers, during many years of closely working with IRBs. We are up to date and in compliance with all regulatory agencies, including the US Food and Drug Administration (FDA).
Services of certified IRBs, including a central IRB when it is recommended by a sponsor, are employed to guarantee quality and transparency of our job.
Also, within our research facility we count with suitable interview rooms to perform the informed consent process in a professional and confidential environment.
Dual enrollment in clinical trials
Ocean Blue Medical Research Center throughout years of experience in clinical research, we are responsive in avoiding duplicate subjects. We implement biometric fingerprint technology and analysis of subject's demographics data to track clinical trial history for every participant.
As a result, we prevent dual enrollment in clinical trials and duplication of volunteers between others research sites in South Florida and Ocean Blue Medical Research Center.
This valuable tool as part of our Good Clinical Practice during the conduction of clinical trial is helping us to achieve three major key factors:
We have partnered with the Collaborative Institutional Training Initiative at the University of Miami - CITI Program - to help doctors and other healthcare specialists to become clinical researchers and build a curriculum vitae according to the rules and regulation established for these practices.
If you have considered, the clinical research avenue in your professional career, the links below provide specific information about the required trainings and certifications we ask in order to apply for a position in our organization either as a clinical research coordinator or principal investigator.
Please do not hesitate to email us with any question!
Ocean Blue Medical Research Center offers and do full-service early phase clinical research and collect data about single and multiples doses, drug interaction, proof-of-concept, bioequivalence, cardiac safety, special populations, therapeutic subspecialties; test of large and small molecules, as well as new and generic compounds.
All data generated are accurate and quickly collected by selecting the most appropriate assay and the latest bioanalytical technologies and recruiting the most appropriate healthy and patient participants and assigning the most experienced clinical teams, including physicians, nurses, scientists and project managers to your study.
The data collected is given to our clients and sponsors for further analysis that help them to make critical decisions when needed.
Our extended experience and professionalism, make of our company your perfect choice in South Florida: comprehensive, flexible, with a great staff, ready to meet all your expectations and needs. Working with us is a rewarding experience either for our clients and sponsors as well as for each volunteer who decides participate of a clinical trial.
Our bilingual team of investigators, sub-investigators, clinical research coordinators and associates, is highly qualified. This enthusiastic group of professionals specifically accumulates more than 30 years of experience in clinical trials and data entry.