A Trusted Partner in Clinical Trial Execution
Florida International Medical Research
Operational Precision for Today’s Clinical Studies.
Focused on operational quality, regulatory compliance, and study performance
Our Commitment to Clinical Research
At Florida International Medical Research, our mission is to support the advancement of healthcare through ethically conducted, high-quality clinical research. We are dedicated to contributing to the development of medical knowledge by collaborating with research partners and upholding rigorous scientific and regulatory standards.
Our work is guided by a commitment to participant safety, data integrity, and responsible study execution. Through carefully designed research processes and experienced clinical oversight, we aim to support clinical studies that help improve treatment options and patient outcomes.
We conduct Phase II–IV clinical trials across multiple therapeutic areas, ensuring high standards of patient care, regulatory compliance, and scientific excellence.
Clinical Team
Our multidisciplinary clinical team is composed of experienced research coordinators, nurses, regulatory specialists, and data professionals dedicated to the successful execution of clinical studies.
Each member of our team is trained in protocol adherence, informed consent processes, participant management, and accurate data documentation. Through structured workflows and continuous training, we ensure consistency, efficiency, and regulatory compliance throughout every phase of each study.
Clinical Operations & Coordination:
Support for study initiation and site activation in alignment with sponsor and CRO requirements
Protocol based study execution, including visit coordination and participant management
Accurate source documentation, data entry, and continuous data quality oversight
Preparation and support for monitoring visits, audits, and study close out activities
How We Support Sponsors and CROs
Operational Performance Indicators
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Strong enrollment performance supported by proactive screening workflows.
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Short average timelines between screening and randomization.
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High participant retention demonstrating effective follow-up and engagement.
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Consistent data completeness and protocol compliance.
Ongoing Training & Certifications
All clinical and operational staff participate in continuous training programs to ensure compliance with evolving regulatory and safety standards, including:
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Annual GCP and SOP training
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HIPAA and OSHA compliance programs
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Emergency response certifications (CPR, AED, ACLS)
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IATA certification for biological sample handling
Sponsor & CRO Collaboration
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Clear communication throughout the study lifecycle
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Coordinated workflows aligned with sponsor expectations
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Timely responses to monitoring and data requests
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Collaborative approach to study execution and reporting
Principal Investigator
Alejandro Danilo Jorrin Simon MD
(Internal Medicine)
At Florida International Medical Research, we are committed to building trusted, collaborative partnerships with sponsors and contract research organizations by delivering robust operational excellence and measurable performance. With a highly experienced research staff, advanced technological capabilities, and a diverse local population to support recruitment, we understand what it takes to achieve recruitment targets and data quality objectives in competitive timelines. Our goal is simple: to offer a research experience that enhances study outcomes while supporting the strategic goals of every sponsor and CRO we serve.
A research environment built to support quality, efficiency, and regulatory compliance.
Connect With Us
Florida International Medical Research
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