A New Kind of Site Management Organization
We do more than manage sites — we rescue, launch, build, and partner to strengthen the entire clinical research ecosystem.
At ICRC, we’re reimagining what a Site Mangement Organization (SMO) can be. We don’t just manage sites. We support every part of the research journey. Whether it’s rescuing underperforming sites, launching new clinical research careers, building research capacity for physicians, or partnering with sponsors and CROs, our mission is simple: empower sites, accelerate trials, and strengthen the future of clinical research.
We believe every research site has the potential to succeed - they just need the right support. With years of experience in site management and clinical operations, our team specializes in helping sites overcome challenges, meet sponsor expectations, and deliver quality data.
Underperforming sites can delay clinical trials, compromise data integrity, and lead to costly compliance issues. Our SMO specializes in site rescue, partnering with Sponsors to improve struggling sites and prevent regulatory risks. We also support private practices and clinics that need additional research expertise, staffing solutions, or operational improvements. By optimizing site performance, we help ensure trials stay on schedule, meet enrollment goals, and deliver high-quality outcomes.
Our Expertise
Our team brings extensive experience in clinical trials, compliance, and site management, led by our founder, Amaka Ndukwe, who has worked in the life sciences industry as a Clinical Research Associate (CRA), Study Coordinator, and Clinical Trial Lead (CL). With decades of experience managing clinical trial sites and leading clinical trial programs, Amaka has witnessed firsthand the challenges faced by underresourced sites and the significant burden they place on Sponsors and CROs.
After years of working closely with challenged sites, Amaka founded this company to bridge the gap between research sites and Sponsors/CROs, ensuring that sites receive the support, training, and operational improvements needed to succeed. Having worked on both sides—as a representative of CROs and Sponsors—Amaka understands exactly what is expected from high-performing research sites. This unique perspective allows our team to implement tailored strategies that enhance site compliance, efficiency, and overall trial success.
Our team comprises experienced Nurse Research Coordinators, Clinical Research Associates (CRAs), and Clinical Trial Assistants (CTAs), all dedicated to supporting research sites in achieving excellence. With hands-on expertise in site operations, patient recruitment, protocol compliance, and regulatory adherence, our staff ensures that challenged sites can meet the rigorous demands of clinical trials.
Our Mission
At Integrated Clinical Research Center (ICRC), we are embarking on a transformative journey to redefine clinical research through powerful collaborations with principal investigators (PIs) and sponsors. Our mission is to empower sites, accelerate trials, and strengthen the future of clinical research by transforming challenged sites into high-functioning research centers. We partner with Sponsors to rescue challenged sites, ensuring compliance, efficiency, and data integrity while also equipping private practices and clinics with the expertise needed to successfully conduct research. By addressing staffing challenges, operational inefficiencies, and regulatory risks, we help ensure clinical trials stay on track, meet enrollment goals, and deliver high-quality outcomes that advance medical innovation.
Our Vision
Our vision is to be the leading force in clinical trial site transformation, ensuring that every research site—regardless of its challenges—can operate at the highest standards of compliance, efficiency, and excellence. We envision a future where sites receive the support they need to further medical advancements, and contribute to high-quality, timely, and impactful clinical research that improves patient outcomes worldwide.