Research Management Partners (RMP) oversees a network of more than 10 fully equipped research sites located throughout Florida and Puerto Rico, all operating under a unified SOP program that ensures the highest standards of regulatory compliance and research quality. Each site adheres strictly to ICH-GCP guidelines, FDA requirements, IRB regulations, and all operational metrics established by our SMO to guarantee audit-ready performance at all times.
 

Collectively, our network brings together a team of more than 50 board-certified physicians and specialists across multiple therapeutic areas, supported by research professionals with over 20 years of uninterrupted experience in clinical trial operations. This extensive expertise allows our sites to manage a wide range of studies—from Phase I to Phase IV—with consistency, accuracy, and full regulatory alignment.
 

RMP sites are committed to delivering high-quality data, ensuring patient safety, optimizing recruitment strategies, and meeting sponsor expectations through standardized procedures, centralized CTMS infrastructure, and continuous oversight from our SMO leadership. This integrated approach ensures operational excellence and positions our network as a reliable, high-performance partner for sponsors and CROs.