Our network is designed to be effective and efficient, and supports expedited patient enrollment. Our investigators attract and retain patients in clinical trials by building patient relationships organically, ensuring patients’ engagement, compliance, and retention throughout the trial. Our Investigative Site Network is augmented by KUR-trained and experienced site-level research staff who are focused on patient recruitment, protocol execution, compliance, and data quality.

Our proprietary database of patient information allows us to securely store patient data and efficiently search our database by age, gender, diangoses, and various inclusion/exclusion criteria. By filtering our database, we can provide sponsors with realistic and accurate enrollment data and tailor our clinical trials to the needs of our patients.

Our dedicated 24/7 quality assurance team consistently monitors data to ensure data quality and integrity. KUR quality professionals remotely evaluate data collection and regulatory documents, review sponsor feedback from recent monitoring visits, and maintain equipment calibration documentation. We provide Sponsors and CROs access to an eSource system for QA and monitoring activities. The data is ready for source verification and external monitoring by the CRA within 24 hours of each subject visit.

We are 95% digital and all clinical trial data is documented through our web-based Clinical Trial Management System (CTMS) to ensure quality, accuracy, and timeliness. With the rising need for remote capabilities within the research industry, our CTMS allows for seamless remote monitoring and real-time quality assurance auditing. By utilizing a CTMS, we can accurately track budgets, costs, and invoices to ensure an accurate financial outcome for each trial.

KUR Research works closely with sponsors to ensure enrollment and retention goals are maintained throughout the duration of the study. One tool we utilize to combat enrollment hurdles is marketing and advertisement. By utilizing IRB-approved marketing materials, we reach qualifying subjects via a variety of digital, print, and social media sources. Marketing and recruitment efforts are done centrally to reduce the burden on the individual sites, so they can focus on protocol execution and data management.

One of the many benefits of working with KUR Research is the streamlined process we utilize for study start-up. Sponsors can expect to execute the CTA and budget for all KUR sites through one department, and all regulatory start up documents will be handled and maintained by a KUR regulatory representative.

We understand that the start-up process is only the beginning of a long-term relationship with our sponsors, and KUR Research ensures an excellent experience from the start.