At Ideal Clinical Research (ICR), our mission is to conduct Phase II–IV clinical trials with unmatched quality, efficiency, and ethical integrity. We are committed to delivering compassionate care while upholding the highest standards of safety, regulatory compliance, and participant satisfaction.
Our team of certified investigators, coordinators, and support staff is passionate about advancing medical research to improve patient outcomes and contribute to the future of healthcare.
Ideal Clinical Research has built a proven track record of success in high-enrollment clinical trials, particularly in vaccine development with renowned pharmaceutical partners such as Moderna, Pfizer, and others.
In addition to vaccines, we actively conduct trials across a broad range of therapeutic areas, including:
Our commitment to data accuracy, protocol adherence, and regulatory excellence ensures the production of credible, high-quality data. To prevent dual enrollment and protect data validity, we utilize VCT (Verified Clinical Trials) biometric scanning — a state-of-the-art system designed to safeguard trial integrity.
We leverage insights from hundreds of completed studies to deliver faster feasibility, smarter enrollment strategies, and seamless startup processes.
Principal Investigator | Internal Medicine
Principal Investigator | Women’s Health
Principal Investigator | Women’s Health
Principal Investigator | Urology
Sub-Investigator
