Reliable Oversight. High-Performing Trial Sites.
At InSight Health Clinical, we support the success of your clinical trial from the ground up, starting with the sites themselves. Our Site Management and Clinical Monitoring services ensure that every research site operates at the highest standard of compliance, quality, and performance.
We combine deep regulatory expertise, local knowledge, and Good Clinical Practice (GCP) to oversee trial operations that are ethical, efficient, and data-driven. Whether we’re managing a single-site pilot or a multi-center study, our monitoring approach is built on consistency, accuracy, and proactive risk mitigation.
What We Offer
Site Selection & Feasibility
We identify and assess trial sites based on patient access, infrastructure, regulatory environment, and past performance, ensuring you launch from the right place, with the right people.
Study Start-Up Coordination
We manage all aspects of trial initiation, including ethics submissions, contracts, site training, and readiness assessments to ensure timely activation.
Routine Monitoring & Reporting
Our Clinical Research Associates (CRAs) conduct site visits to verify protocol adherence, data accuracy, source documentation, and patient safety—reporting findings in real time.
Compliance & Quality Assurance
We ensure full compliance with ICH-GCP, local regulations, and sponsor SOPs through standardized checklists, deviation tracking, and continuous improvement support.
Site Performance Optimization
From recruitment tracking to staff coaching and retention strategies, we help improve performance metrics and reduce site-level trial delays.