Research Management Partners

Embedded research. Predictable execution.

One partner across sites, with consistent trial operations from start-up to closeout.

Our approach

Research embedded in practices. Oversight that keeps protocols moving.

Research Management Partners is a Site Management Organization for sponsors and CROs that need accelerated start-up, reliable recruitment, and consistent quality across a multi-specialty network — with centralized operational support inside clinics patients already trust.

Engineered for clinical speed and protocol integrity.

Rapid study start-up

Regulatory and operations teams work in parallel on contracts, submissions, and site readiness so activation does not stall on paperwork. Sponsors get a clearer path from feasibility to first patient in, with the same process applied across the network.

Diverse patient populations

Embedded sites with direct access across specialties and communities.

Single point of contact

Centralized communication that reduces administrative load for sponsors and CROs.

Centralized quality

Standardized SOPs, training, quality oversight, and performance monitoring.

Scalable multi-site execution

Whether the protocol needs a single embedded clinic or a regional multicenter program, RMP keeps investigators, SOPs, and reporting under one operating model. That consistency reduces sponsor coordination load as the study grows from pilot sites to broader enrollment.

Network scale

Capacity that supports multicenter execution.

Confirmed operating scale across sites, investigators, and Phase I–IV experience — the foundation sponsors and CROs review before feasibility.

100+

Research sites

150+

Investigators and sub-investigators

I–IV

Clinical trial experience

Multi

Specialty network

Interactive estimator

Study Impact Timeline

Select phase and site scale to see planning ranges grounded in RMP’s published operational signals — IRB timing, centralized activation, and network capacity.

Study phase

Sites required

Phase IV · 1–5 sites 100+ sites · 150+ investigators

Est. IRB window: 7–12 days
Avg. site activation speed: 21–42 days
Centralized reporting model: 67%
Screening readiness: First weeks

Planning estimates only — not a contractual SLA. Formal feasibility confirms protocol-specific timelines.

Request Feasibility

Therapeutic experience

Multi-specialty medical expertise

Research Sites

Bring research into a practice patients already trust.

Established clinics can offer trials without standing up a full research department. RMP centralizes operations, quality, start-up, and ongoing study support so investigators stay focused on patient care while sponsors gain a reliable, scalable partner across the network.

Outcomes

Directly aligned with your protocol KPIs

Operational workflows built specifically to accelerate site activation, optimize enrollment, and deliver clean data.

Faster site activation

Experienced regulatory and start-up teams at the site level.

Stronger patient recruitment

Direct access to established practice populations.

Improved patient retention

Care delivered inside trusted community practices.

Consistent protocol compliance

Shared SOPs and centralized quality oversight.

Schedule Call

Ready to accelerate your next study?

Connect with clinical operations to review capabilities, discuss site selection across our 100+ site network, and align on Phase I–IV feasibility.

Or reach the Miami office at 786-464-0868 · rrios@rmpsmo.com

How sponsors work with RMP

Feasibility

One partner reviews protocol fit across the network and surfaces ready investigators.

Start-up

Regulatory and contracts move in parallel so activation is not waiting on paperwork.

Enrollment

Embedded practices open access to diverse patient populations under shared SOPs.

Oversight

Centralized quality and a single point of contact keep multi-site execution consistent.

FAQs

Answers about how Research Management Partners supports sponsors, CROs, and research sites — from embedded trial operations to centralized oversight across Phase I–IV.

What does Research Management Partners do?

RMP is a Site Management Organization. We provide centralized operational oversight, accelerated study start-up, and consistent trial execution across a growing network of research sites.

How does embedded research work?

Trials run inside established medical practices patients already trust. Investigators keep clinical leadership while RMP centralizes operations, quality, training, and sponsor communication.

How large is the RMP network?

The network includes 100+ research sites and 150+ investigators across a multi-specialty practice base, supporting scalable single-site and multi-site programs.

Which trial phases do you support?

RMP supports clinical research across Phase I–IV, with processes built around activation speed, recruitment, retention, protocol compliance, and data quality.

How do sponsors and CROs work with RMP?

You get a single operating partner for feasibility, start-up, enrollment, and oversight. Regulatory and contracts move in parallel so activation is not blocked by paperwork, with shared SOPs across sites.

Can an established clinic join as a research site?

Yes. RMP is built for practices that want to offer trials without standing up a full research department. We supply centralized operations and quality support while physicians remain investigators.

Which therapeutic areas do you cover?

The network spans multi-specialty expertise — including internal medicine, cardiology, endocrinology, pulmonology, gastroenterology, psychiatry, neurology, dermatology, rheumatology, infectious disease, women’s health, and a dedicated oncology research module.

How do I schedule an introductory call?

Use the Schedule Call form above, call the Miami office at 786-464-0868, or email rrios@rmpsmo.com. The office is at 11980 SW 144th Ct. Suite 209, Miami, FL 33186.

Contact

Reach clinical operations directly.

Prefer a call, email, or the Miami office? Use the channels below — the same details as our Contact page.

Phone

Speak with the Miami office about capabilities, feasibility, or an introductory call.

Email

Send protocol questions or partnership inquiries to clinical operations.

Miami office

11980 SW 144th Ct. Suite 209 Miami, FL 33186

Schedule a call

Use the form above, or open the full contact page for the same office details.