Your Partner for Immunology Clinical Trial Management

Immunology research is evolving at a rapid pace. From the rise of mRNA vaccines to the expanding role of biologics, clinical trials in this space must balance scientific advancement with complex operational demands. At Remington-Davis (RDI), we’ve supported these trials for decades, pairing deep therapeutic expertise with a patient-centered approach to help drive success.

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How we help immunology clinical trials succeed

Immunology trials often involve complex eligibility criteria, long-term treatment protocols, and patients managing chronic or fluctuating symptoms. At RDI, our experience with these challenges has shaped a service model that combines responsiveness and adaptability with consistency, helping sponsors and CROs meet study timelines while sustaining participant engagement.

Patient Recruitment
Patient Management
Data Collection
Regulatory Compliance

Patient Recruitment

We maintain a database of more than 19,000 prescreened volunteers, including individuals with prior experience in immunology studies. This allows us to quickly identify target patients for trials in areas such as autoimmune disease, allergic conditions, and vaccine development. Our outreach efforts prioritize inclusivity and community engagement, which contributes to a participant pool that reflects populations most affected by many immune-mediated conditions.

Patient Management

Once enrolled, patients benefit from a study experience designed to reduce friction and encourage long-term participation. We offer flexible scheduling, including availability outside of standard business hours, and arrange transportation for those with access challenges. For longer visits, our facility provides private rooms equipped with comfort amenities. These accommodations are part of a broader effort to make sure participants always feel supported.

Data Collection

We understand the data demands of immunology trials, from serial blood draws to symptom tracking to complex dosing schedules. Data is entered into our electronic systems the same day it is collected, enabling real-time visibility and prompt query resolution. Our site also supports hybrid and decentralized trial models, including ePRO capture and telehealth components, which can help broaden access and improve compliance.

Regulatory Compliance

Regulatory oversight is a critical element of immunology research, especially when protocols involve investigational biologics, immunosuppressive agents, or novel vaccine platforms. Our in-house regulatory team works closely with sponsors and CROs to maintain full compliance with ICH-GCP standards and study-specific requirements. From IRB submission to site close-out, our clinical development approach emphasizes accuracy, transparency, and responsiveness.

Highlights of our extensive trial expertise

30+ Years

of experience managing trials

19,000+

patients in our database

Nearly 37%

diversity rate

97%

patient retention rate

Interested in participating in a study?

Discover the latest RDI studies that are currently enrolling, learn more about their focus, and find out how you can participate in groundbreaking research.

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Trial management expertise in a patient-centric environment

Immunology trials often ask more of both patients and protocols: longer visits, more intensive monitoring, and heightened attention to participant well-being. Our 7,500-square-foot facility in Columbus, Ohio was built to meet these needs with a balance of technical capability and patient-centered design.

Within our space, sponsors and CROs will find dedicated exam and infusion rooms suited to complex procedures, as well as private areas for pharmacokinetic sampling, serial ECGs, or extended observation periods. Onsite lab processing and centralized data management help maintain the pace and precision required for today’s immunology studies.

Equally important is the environment we create for participants. From first visit to final follow-up, our goal is to offer a setting that feels calm, accessible, and respectful. The result is a high-touch trial experience that supports protocol adherence and patient retention — whether the study involves an investigational biologic, a decentralized visit model, or both.

What industry professionals have to say about working with RDI

“If a company doing a performance study asks me for a recommended clinical trial site, RDI would be the first one I think about. They offer very good service in an ideal setting.” - Shoshana Friedman, VP of Clinical & Regulatory Affairs

Partner with us for your next immunology disease trial.

At Remington-Davis Clinical Research, we are committed to supporting you with trusted clinical research services. Schedule a 30-minute consultation with us to discuss your clinical trial management challenges and learn how we can help.

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