Sunbeam Clinical Research is a Site Management Organization (SMO) headquartered in Prosper, Texas, specializing in the coordination and management of Phase II–IV clinical trials across the Dallas–Fort Worth Metroplex and Southern Oklahoma.

We partner with Sponsors, CROs, and Principal Investigators to deliver high-quality research across multiple therapeutic areas including Cardiovascular, Neurology, Nephrology, Gastroenterology, Psychiatry, Infectious Disease, and Primary Care.

Our services span the full trial lifecycle from site activation and IRB submissions to patient recruitment, regulatory document management, source data verification, and study closeout. We operate as a fully paperless organization, utilizing industry-leading EDC platforms including Medidata Rave, and maintain strict compliance with GCP, ICH, and FDA regulations including 21 CFR Parts 11 and 50.

Founded in 2017, Sunbeam manages an established network of 17+ clinical sites staffed by medically trained CRCs and regulatory professionals committed to data integrity and protocol adherence.

Whether you are a Sponsor seeking qualified sites or a physician interested in becoming a Principal Investigator, Sunbeam provides the infrastructure, expertise, and accountability to conduct research at the highest standards.


Sunbeam Clinical Research

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Sunbeam Clinical Research

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