Capabilities

Revolutionizing Community Research: Your Partner in Diverse Clinical Trial Success

At Lumi Research, we specialize in navigating the complexities of launching clinical trials in community settings, transforming challenges into opportunities for impactful research and enhanced diversity. From initial sponsor outreach and rapid budget finalization to accelerated study activation, our expert team manages every intricate detail. We don’t just streamline the process; we build bridges, ensuring cutting-edge research reaches underserved populations and drives meaningful advancements in health equity, faster.

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What We Do

Lumi Research Group provides full-service clinical trial management with a focus on efficiency, quality, and access. We oversee every stage of the research process — including regulatory and IRB submissions, patient screening and enrollment, source documentation, data entry, and query resolution. Our contracts and budget team brings extensive experience, completing over 100 budgets across various specialties with an average turnaround of just 2–4 weeks. We also manage specialty billing and streamline contract execution to reduce startup delays and keep studies on track.

Seasoned Principal Investigators with experience in over 77 combined trials

Clinics within the greater Houston, Dallas and Fort Worth communities

Patients will receive access to clinical trials within the network

Month Average Study Start-Up Time

Expanding Access Through Community Partnerships

Beyond operations, Lumi drives trial growth through strong relationships with sponsors, CROs, and medical science liaisons. We identify new study opportunities, develop and support research-ready sites, and provide training for new investigators from within the community. Our foundation in oncology includes an average of 13 activated trials per year and a patient base of more than 5,000. With experienced research staff embedded at each site and centralized support from our fully equipped headquarters, we reduce administrative burden and deliver startup timelines as fast as 10 days — ensuring clinical trials are accessible to every provider and patient, no matter the setting.

Oncology

We are deeply focused in Oncology, supporting a wide range of cancer indications, while also maintaining proficiency in other therapeutic areas such as: