About Us

Accelerating Access.
Advancing Equity.
Anchored in Community.

Our Mission

Bridging the Gap Between Innovation and Inclusion

DMV Clinical Trials is a clinical research site network dedicated to improving access to cutting-edge clinical trials across the Washington DC, Maryland, and Virginia region. We partner with sponsors, CROs, and physician practices to bring Phase 1–4 trials directly into communities that are historically underserved in research.

At DMV CTs, we are driven by a dual commitment: scientific excellence and health equity. Our team of experienced clinical research professionals, investigators, and community health advocates ensures high-quality trial execution from feasibility to close-out, with a focus on culturally responsive recruitment, retention, and patient care.

Founded in the heart of the DMV region, we understand the unique health challenges and demographics of our community. We believe that every person — regardless of race, ethnicity, income, or zip code — deserves access to the most advanced medical treatments available.

Research coordinator with participant
Our Values

What Guides Everything We Do

Health Equity

We are committed to ensuring that clinical research reflects the diversity of the communities it serves. We actively recruit from historically underserved populations and partner with community organizations to remove barriers to participation.

Scientific Excellence

Every protocol we execute meets the highest standards of Good Clinical Practice (GCP). Our team of experienced investigators and coordinators ensures rigorous data quality and participant safety at every step.

Community Partnership

We are not just a research site — we are a community partner. We build long-term relationships with local organizations, faith communities, and healthcare providers to embed research into the fabric of the DMV region.

Transparency & Trust

We believe that trust is earned through transparency. We communicate openly with participants, provide plain-language information about all studies, and maintain the highest standards of informed consent.

Our Capabilities

Full-Service Clinical Research Site

Phase 1 – 4 clinical trial execution
IRB-approved protocols
Certified Clinical Research Professionals (CCRP)
Culturally responsive recruitment strategies
Electronic data capture (EDC) systems
Biospecimen collection and processing
Participant retention programs
Regulatory submission support
Clinical research laboratory

Ready to Partner With Us?

Whether you're a sponsor, CRO, physician practice, or prospective participant — we'd love to hear from you.