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clinical focus

Improved Health Outcomes

Clinical Expertise & Experience

Why Choose Us?
Your Trusted Partner for High Quality, Inclusive Clinical Trials

At Research by Design, we expertly conduct clinical trials using state-of-the-art research technology through a centralized, physician-led site network specialized in nephrology, urology, hepatology, optometry, and internal medicine. Our commitment to diversity drives inclusive participation by expanding access to underserved and underrepresented communities.

From study startup to closeout, we provide comprehensive, full-service support focused on transparency, regulatory excellence, and collaborative execution. Our efficient processes reduce delays and improve delivery, enabling Sponsors and CROs to meet timelines without compromising quality or compliance.

We expanded our overnight pharmacokinetic (PK) clinical unit capacity to 28 beds in 2025 to meet increasing sponsor demand. View our PK Unit Tour for details on the accommodations and layout.

For over 20 years, our diverse team of medical professionals has provided consistent, high-quality research in a professional and ethical manner through collaboration with multi-national pharmaceutical, biotechnology and CRO companies on Phase I-IV clinical trials. Research by Design has successfully conducted more than 140+ clinical trials across a broad range of therapeutic areas. Our board-certified investigators and experienced research team operate in strict compliance with Good Clinical Practice (GCP) and stay at the forefront of evolving medical technologies and clinical research standards. Through efficient, cost-effective trial management, we deliver high-quality data that helps accelerate sponsor timelines and support regulatory approval.

 

Clinical Trials

Research by Design has conducted more than 140+ clinical trials across a broad range of therapeutic areas

participant access

With access to over 20,000 patient records, we have an excellent recruitment and retention rate.

REGULATORY & COMPLIANCE

We utilize 21 CFR Part 11 compliant
eRegulatory and eSource digital
platforms and a multitude of EDC and IWR systems.


PARTNER WITH US ON YOUR NEXT CLINICAL TRIAL

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Clinical Trial Expertise