Partners to the site.

Modeli Research Consultants is a clinical research consulting firm based in Florida. We were built by people who have worked at the site level, so we work alongside your team the way we'd want a partner to work with us: on call, hands on, and in it for the long term.

Our mission is to drive research site success.

We do it through expert regulatory and quality compliance, providing the guidance and support that keep standards high and operations running smoothly. Everything we do is grounded in integrity and excellence, with one goal: to strengthen your research business.

Assuring regulatory compliance

Our compliance specialists guide you through every step so your studies meet the highest standards and stay ethical and safe.

Experience and professionalism

Our expertise spans regulatory compliance, clinical operations and trial management, and we bring it to every project.

Experts who care

We know what sites face. We give you the support, resources and guidance to meet regulatory requirements with confidence.

Leadership

MRC is led by people who work inside research sites every week, and backed by a team of clinical research consultants.

Simon Gomez

Founder and Chief Executive Officer

RQAP-GCP, ACRP-CP

Simon founded Modeli Research Consultants and leads its audit, quality and regulatory work with research sites. He brings what he learns on the front lines of quality assurance, including FDA and BIMO insight from the Society of Quality Assurance, back to the sites MRC supports, so every client benefits from current inspection experience.

Vice President, ACRP Southeast
Institutional review board member
Member, Society of Quality Assurance (SQA)

Randy Rivas

Director of Regulatory Compliance

Regulatory affairs specialist

Randy is a regulatory affairs specialist and MRC's go-to expert on clinical research regulations. He leads regulatory compliance across our client sites, working alongside study teams to keep each site aligned with FDA and ICH GCP requirements. His focus is catching compliance gaps early, long before a monitor or inspector does.

FDA and ICH GCP regulatory expertise
Regulatory affairs and compliance oversight
On site with client study teams

Backed by a team of clinical research consultants.

Our consultants work alongside your study teams, on site and on call, with hands-on experience across every part of running a study. Each engagement is staffed with the specialists your studies need.

Regulatory
Quality assurance
Clinical operations
eSource and CTMS
Budgets and contracts
Training and SOPs

MedLaunch

Connecting ambitious students with impactful research opportunities to shape the future of medicine.

Apply to MedLaunch

Work with us

Looking for a partner who knows research sites from the inside? Tell us about your site and your studies.

Better together.

Tell us where your site needs support. We'll talk it through and show you how we can help.

Book a consultation

(786) 383-6661 simon@modeliresearch.com