Research Sites

Multi-State Research Site Network Across the U.S. and Puerto Rico

One SOP program across Florida and Puerto Rico

Research Management Partners (RMP) oversees a network of more than 100+ 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.

100+

Fully equipped research sites

FL & PR

Geographic coverage

Unified

SOP program across the network

Audit-ready

SMO operational metrics

Regulatory alignment

Built for compliance and research quality

Sites follow the standards that keep studies inspection-ready — the same framework our SMO uses to govern day-to-day performance.

ICH-GCP

Guidelines applied across site operations

FDA

Requirements adhered to at every site

IRB

Regulations followed for study conduct

SMO metrics

Operational measures for audit-ready performance

People & experience

Investigators and operations depth behind every site

Collectively, our network brings together a team of more than 150+ board-certified physicians and specialists across multiple therapeutic areas, supported by research professionals with over 35 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.

150+

Board-certified physicians and specialists

35+

Years of uninterrupted clinical trial operations experience

I–IV

Study phases managed across the network

Site operations

How RMP sites deliver for sponsors and CROs

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. Our integrated approach ensures operational excellence and positions our network as a reliable, high-performance partner for sponsors and CROs.

High-quality data

Standardized procedures that support clean, reliable study data.

Patient safety

Site conduct oriented to protect participants throughout the trial.

Recruitment optimization

Strategies that help sites meet enrollment expectations.

Centralized CTMS

Infrastructure that keeps operations visible and coordinated.

SMO leadership oversight

Continuous oversight from RMP leadership across the network.

Sponsor expectations

An integrated model built for high-performance partnership.

Why Sponsors Choose RMP

What our research teams support

Our dedicated research teams work closely with Sponsors and CROs to support:

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