ClinAssure currently provides monitoring services to support clinical trials in the United States, Canada, and Mexico. Our Clinical Research Associates (CRAs) offer a wealth of therapeutic expertise and clinical research experience. Our monitoring teams work to manage and develop productive relationships with sites through strong communications, organizational skills, and in-depth knowledge of regulatory compliance.

Regional Monitoring Our CRAs are experienced professionals who perform monitoring activities to ensure strict adherence to all regulatory requirements and study protocols. They are also dedicated to establishing strong relationships with our investigative sites to ensure successful study progress. By working onsite with our clients, it improves the consistency of project management. It also ensures that the sponsor gets consistent, high-quality monitoring. Our centralized decision making model allows us faster start-up mode, lower coordination costs, and most importantly, allows us to remain an integrated part of your project team. ClinAssure will work with sponsors on their trials to select and place experienced CRAs in close proximity to all of the sites for efficiency.  All of our monitors have a minimum of five years of regional monitoring specific experience. We strive to minimize the number of studies assigned per CRA to maximize their project ownership and efficiencies while balancing the amount of travel.

For more information about ClinAssure’s centralized monitoring services, contact us at 949.502.6001.