MonitorCRO provides high-quality, cost-effective, and reliable services as a pioneering contract research organization with two decades of experience. From start-up to close-out, our team works in collaboration for every project.
We deliver what we promise! We meet study timelines in all phases of clinical studies through meticulous planning and organization supported by targeted SOPs. We are here to help you in every step of the way, from study design, protocol development and completion of a series of clinical trial documentation to regulatory approvals and training study teams and sites.
Our professional teams apply their regulatory, operational and data management expertise to consistently solve the challenges which may arise during clinical trials.
High-quality and accurate data collection, analysis, and management are critical during the study run and our data management team ensures that your data is safely collected and safely kept.
Our project managers provide leadership, operational expertise, and accurate execution of all protocol requirements in a timely and cost-effective manner.
Their Scope of Responsibilities Includes:
Primary Liaison with Clients
Team Management (Internal and External)
Project Status Reporting
Our experienced clinical operations teams ensure proper conduct of study, patient safety, and data quality. They instigate good communication between study sites and sponsors.