Community-Based Clinical Research · Miami, FL

Bridging science and the communities that need it most.

My Community Research Center is a trusted, community-based clinical research site advancing innovative therapies through inclusive, ethical, and high-quality study conduct — serving sponsors, physicians, and patients across South Florida.

Site Profile

Strategically located in the heart of South Miami's medical corridor.

Conveniently positioned within the South Miami and Coral Gables corridor, our site provides immediate access to emergent healthcare support and regional medical resources — enhancing participant safety and study reliability.

Just nine minutes from Miami International Airport and adjacent to the Palmetto Expressway, the site is equally accessible for participants and sponsor monitors.

0.5 mi

Keralty Community Hospital

Closest acute-care facility for emergent participant support.

1.5 mi

Nicklaus Children's Hospital

Main campus, providing pediatric specialty backup when required.

3 mi

Coral Gables Hospital

Full-service hospital within the immediate medical corridor.

3 blocks

MD Now Urgent Care

Walking distance for non-emergent assessments and overflow.

Vision Statement

To be a trusted leader in community-based clinical research — advancing therapies through inclusion, ethics, and excellence.

We strive to bridge the gap between science and underserved populations by fostering strong partnerships with sponsors, physicians, and patients — ensuring access to cutting-edge treatments that improve health outcomes for all.

Commitment to Sponsors

A partnership built on rigor, readiness, and results.

Sponsors choose My Community Research Center because we deliver more than completed case-report forms. We deliver clean data, diverse populations, and a team that anticipates challenges before they appear.

01

Operational Excellence

Timely, accurate, and compliant data through streamlined processes and proactive communication.

02

Diversity in Enrollment

Proactive recruitment from underrepresented populations to support inclusive, generalizable research.

03

Quality Assurance

The highest standards of Good Clinical Practice (GCP), regulatory compliance, and patient safety.

04

Site Readiness

A highly trained team and robust infrastructure supporting rapid study activation and execution.

05

Collaborative Partnership

Close alignment with sponsors and CROs to anticipate challenges and ensure successful outcomes.

Core Values

The principles that shape every protocol we execute.

Integrity

Transparency, accountability, and ethical conduct in every trial.

Quality

Precision and consistency in protocol execution and data management.

Patient-Centeredness

Respectful, informed, and inclusive participant care.

Diversity & Inclusion

Authentic representation of underserved communities in research.

Collaboration

Open, transparent communication with sponsors and CROs.

Innovation

Embracing technology and continuous improvement.

Education

Ongoing training and professional development for all staff.

Research Staff

A multi-disciplinary team built for complex protocols.

Board-certified investigators across seven specialties supported by a fully cross-trained clinical, regulatory, and operations team.

Board Certified Jorge Diaz Valdés, MD Internal Medicine · Principal Investigator
Board Certified Richard Pérez Pérez, MD Internal Medicine · Principal Investigator
Board Certified Cesar E. Guerrero, MD Neurology · Principal Investigator
Board Certified Jose H. Suarez, MD Family Medicine · Principal Investigator
Board Certified Manuel J. Hernández, MD Pulmonology · Principal Investigator
Board Certified Luis E. Bermúdez, MD Endocrinology · Principal Investigator
Board Certified Monica Vega, MD Psychiatry · Principal Investigator
Alba M. O'Bourke, MDFamily Medicine · Sub-Investigator
Lizette Vazquez, ARNPSub-Investigator / Rater
Mario Miguel Gomez, APRNResearch Nurse · Coordinator · Rater
Victor A. Ramallo, RNResearch Nurse · Coordinator · QA Backup
Lazaro Llanes, MACoordinator Manager · Data Entry
Yoselin Torres, MAMedical Assistant · Phlebotomist · Lab Coordinator
Sandra Ramallo, MAStudy Coordinator · Data Entry · Regulatory
Maydelis Lugo, BBAStudy Coordinator · Regulatory Assistant
CCRC · ACRP-CP Maida R. Ramallo, FMD CEO · Research Director · Quality Control
Leonardo Ramallo, BSc, BBA Budget & Contract Specialist
Jonathan Ramallo Recruitment & Marketing Coordinator
Alejandro Ramallo, BBA IT & Systems Administration
Trial Execution Performance

Numbers earned over twelve Phase II–IV trials in five years.

A strong enrollment history, low screen-failure rates, and rapid study start-up — driven by a sustained focus on participant engagement, compliance, and protocol fidelity.

45–60 Average enrollment per study
250 Highest single-study enrollment (COVID-19 vaccine)
95% Average participant retention rate
8–10% Average screen-failure rate
7–10 Business days, ICF to first randomization
12 Phase II–IV trials over the past 5 years
Metrics reflect aggregated performance across our active and recently completed clinical trial portfolio. Our team maintains a strong focus on participant engagement and compliance to optimize retention.
Capabilities

Trained, equipped, and audit-ready from day one.

From GCP and ICH E6 (R3) currency to CLIA-waived in-house testing, every operational layer is designed for fast study activation and reliable execution.

Training & Operational Readiness

  • GCP, ICH E6 (R3), and HSP training current for all staff
  • Active SOP training and documentation
  • IATA certification for compliant specimen shipping
  • Experience across multiple EDC and IVRS/IWRS platforms
  • Skilled in EKGs, blood draws (including PK), IV administration, vital signs, and IP handling
  • Capable of conducting home, remote, and virtual study assessments
  • Active Federal Wide Assurance (FWA00034069) valid through January 26, 2029

Research Infrastructure

  • CLIA Waiver Certified
  • −20°C and −70°C freezers for sample storage
  • Refrigerated centrifuge, site-owned EKG, and AED — all annually calibrated
  • Double-locked, temperature-controlled, and digitally monitored IP storage room
  • Three physical exam, EKG, and phlebotomy rooms
  • Private consultation rooms for consenting and assessments
  • Dedicated monitor area with Wi-Fi, phones, and printer/scanner access
  • Welcoming reception area and daily digital temperature monitoring
Previous Collaborations

Trusted by leading sponsors, CROs, and research networks.

Our portfolio reflects collaborations across multiple therapeutic areas and study phases — demonstrating reliability, performance, and a sustained ability to meet the standards of global clinical research partners.

Contract Research Organizations

  • Parexel
  • ICON
  • INC Research
  • Syneos
  • CromSource
  • Premier Research
  • Novella Clinical
  • PPD
  • ClinChoice
  • Oculus
  • Medpace
  • IQVIA
  • Quintiles

Sponsors

  • Merck & Co.
  • Astellas
  • Pfizer
  • Sanofi
  • Mundipharma Research
  • Celgene Corporation
  • Incyte Corporation
  • Foamix
  • Mylan
  • Pharmacosmos
  • Marius Pharmaceutical
  • Brickell Biotech
  • Affibody
  • Philips
  • Axsome Therapeutics
  • IBSA Institut Biochimique
  • GSK
  • Karuna Pharmaceuticals
  • Bristol Myers Squibb
  • Pearl Therapeutics
  • AbbVie Pharmaceutical
  • Novo Nordisk
  • Botanix Pharmaceuticals

Site Network

  • Society for Clinical Research Sites (SCRS)
Partner With Us

We welcome sponsors and CROs committed to innovation, integrity, and inclusive research.

Address
7480 Bird Road, Suite 400
Miami, FL 33155
Phone
305-667-1080
Fax
305-397-2671

Regulatory & Compliance

All staff training and certifications are maintained current and verifiable upon request.

GCP ICH E6 (R3) HSP IATA CLIA Waiver
FWA00034069 Active Federal Wide Assurance, valid through January 26, 2029.