Our Services

RMP connects affiliated physicians directly with leading pharmaceutical sponsors, biotechnology companies, CROs, and medical device organizations. We manage all communication and proactively introduce your site to companies seeking qualified research partners, increasing visibility, credibility, and opportunities to participate in high-value clinical trials.

To support studies requiring additional expertise, RMP can provide Principal Investigators, Sub-Investigators, raters, and therapeutic-area specialists. This expanded medical support helps sites qualify for more complex trials and increases their capacity to participate across multiple therapeutic areas.

We provide complete study start-up support, including feasibility assessments, timeline management, IRB submissions, regulatory documentation, SOP development, and pre-SIV preparation. Our structured approach ensures your site is fully compliant, well-organized, and prepared to meet sponsor and regulatory expectations from day one.

We help sites develop, update, and standardize SOPs to ensure alignment with FDA, ICH-GCP, and IRB requirements. By strengthening internal quality systems and refining workflows, RMP elevates your site from basic operations to a fully structured, compliant, and high-performing research center.

RMP provides complete guidance and oversight for research staff, including coordinator training, quality control processes, documentation support, and protocol adherence monitoring. When needed, we can also supply experienced Clinical Research Coordinators to ensure consistent, sponsor-aligned performance.

RMP handles all budget negotiations on your behalf, ensuring fair compensation for procedures, staff time, and overhead. We protect your financial interests, maximize study-related revenue, and secure clear payment schedules aligned with study milestones. Our financial expertise allows physicians to focus on patient care while we manage the business side of research.

RMP continuously works to strengthen your site’s competitiveness by improving operational infrastructure, enhancing regulatory readiness, expanding therapeutic capabilities, and preparing strong feasibility responses. Our goal is to position your site as a high-performing partner capable of securing diverse and high-value clinical trials.

RMP offers full implementation of RealTime CTMS, including system setup, role assignments, study configuration, eSource and eReg integration, and ongoing support. This powerful platform enhances efficiency, ensures accurate documentation, and keeps your site audit-ready throughout the trial lifecycle.

Once a study begins, RMP offers ongoing operational support including sponsor communication, visit coordination, protocol compliance oversight, regulatory management, timeline monitoring, and audit preparation. This enables physicians to focus on clinical care while we manage the day-to-day execution of the trial.