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Embedded Site Management Organization Supporting Sponsors, CROs, and Clinical Research Sites Through Continuous Oversight and Operational Support
Research Management Partners | Powered by Physician Management Partners
SMO-MSO
“A Fully Integrated SMO-MSO Network Delivering Predictable Start-Up, Reliable Enrollment, and Centralized Quality Across All Sites.”
KEY DIFFERENTIATORS
“We offer the structure of a large network with the flexibility and patient access of independent practices.”
INTEGRATION
Fully affiliated research sites under a single SMO governance model.
OVERSIGHT
PREDICTABILITY
INTEGRITY
ACCOUNTABILITY
Real-time, on-site Quality Control with immediate CAPA execution
Predictable IRB and site activation timelines
Clean, audit-ready data across
Phase I-IV trials
Single point of accountability for multi-site programs
ABOUT US
Research Management Partners (RMP) is a U.S.-based Site Management Organization operating a fully integrated and centrally governed clinical research network.
We enable Sponsors and CROs to reduce execution risk and operational variability by delivering standardized processes, real-time quality oversight, and consistent site performance across all locations.
Our model ensures reliable start-up timelines, strong enrollment execution, and audit-ready data—making RMP a strategic partner for scalable, multi-site clinical trials.
We provide direct access to high-performing research sites and experienced investigators across multiple therapeutic areas, supported by an integrated infrastructure designed to ensure quality, compliance, and consistent delivery at every stage of the study lifecycle.
Network Metrics & Operational Performance
Research Management Partners (RMP) operates a growing clinical research network supported by Physician Management Partners, providing access to diverse patient populations and experienced investigators across multiple therapeutic areas.
Our operational model focuses on predictable timelines, centralized oversight, and consistent quality standards across all affiliated sites.
Network Overview
• 30+ affiliated clinical research sites across Florida and Puerto Rico,
As our network expands across the United States, RMP maintains a continuous “boots-on-the-ground” presence within affiliated sites, actively supervising study conduct, enforcing standardized SOPs, and operating an internal quality control network to ensure regulatory compliance and data integrity.
• 70+ physicians and sub-investigators within the network
• Access to a large and diverse patient population through affiliated medical practices
• Experience supporting Phase I–IV clinical trials
• Multispecialty investigator network covering major therapeutic areas
Operational Capabilities
• Centralized regulatory and quality oversight
• Standardized SOP framework across sites
• Rapid feasibility response and site activation readiness
• Structured patient recruitment through clinic networks
• Continuous monitoring of quality and protocol adherence
This integrated model enables RMP to deliver predictable timelines, consistent quality oversight, and reliable enrollment performance for sponsors and CRO partners.
Therapeutic Areas & Investigator Expertise
Research Management Partners (RMP) operates a multispecialty investigator network with experience supporting Phase I–IV clinical trials across a wide range of therapeutic areas.
Through our affiliated physicians, specialty clinics, and embedded SMO oversight model, our network can support interventional, observational, and biospecimen collection studies across diverse patient populations.
Core Therapeutic Areas
• Psychiatry
• Neurology
• Gastroenterology
• Pulmonology / Respiratory Diseases
• Rheumatology
• Dermatology
• Endocrinology / Metabolic Disorders
• Cardiovascular Diseases
• Nephrology
• Internal Medicine
• Infectious Diseases
• Immunology
Additional Clinical Research Areas
• Oncology / Hematology
• Pain Management
• Sleep Disorders
• Allergy and Immunologic Disorders
• Women’s Health / Gynecology
• Men’s Health
• Urology
• Pediatrics
• Geriatric Medicine
• Rare Diseases
• Autoimmune Diseases
• Metabolic and Obesity Disorders
Types of Studies Supported
• Phase I Clinical Trials
• Phase II Clinical Trials
• Phase III Clinical Trials
• Phase IV Post-Marketing Studies
• Device Trials
• Observational Studies
• Real-World Evidence Studies
• Epidemiological Studies
• Biospecimen and Sample Collection Studies
• Registry Studies
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Our integrated research infrastructure and continuous site oversight allow us to maintain consistent quality standards while supporting sponsors and CROs across a broad spectrum of clinical development programs.
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