We are committed to recruiting high-quality, reliable participants through a rigorous enrollment validation process. This includes VCT with biometric verification, checks to ensure no prior study involvement, clear participant education during pre-screening, and safeguards to prevent duplicate or cross-site enrollment
At Ideal Clinical Research (ICR) we understand that timely and effective enrollment drives the progress and success of clinical trials, and we’ve built a proven infrastructure to support it.
Our recruitment capabilities are supported by direct access to a robust patient population. Through our network of Principal Investigators (PIs) and Sub-Investigators (Sub-Is), we have access to over 32,000 patients via their private practices. This built-in access allows us to rapidly identify eligible participants across multiple therapeutic areas.
In addition to our practice-based patient pool, ICR maintains an internal, database of clinical research participants. This registry includes individuals with prior research experience and patients who have expressed interest in participating in future studies, allowing us to accelerate outreach and screening efforts with compliant subjects.
Our recruitment team takes pride in consistently meeting—and often exceeding—sponsor enrollment goals. We attribute this success to our proactive planning, patient-first approach, and transparent communication with sponsors.
We utilize a wide range of communication tools to stay engaged with our community and patient base, including:
These tools help us maintain long-term relationships with potential participants and keep them informed about new and ongoing studies.
We provide:
