DSP

Services

Site Monitoring

DSP's site monitoring services include site selection, site initiation, interim, and final site visits.

Additionally,  tailored CRA training services include SOPs, GCP/ICH guidelines, CRA operations manual, therapeutic area training, CTMS software, and EDC training.

All DSP site monitors are highly qualified clinical research professionals and are experienced in multiple therapeutic areas. Our monitors are responsive and flexible, and skilled at adapting to a variety of SOP practices and corporate cultures.

• More than 60% of our Monitors have a background in nursing and 50% have advanced degrees
• All our monitors are required to be Certified Clinical Research Associates (CCRA) with the Association of Clinical Research Professionals (ACRP)
• Our monitors average ten years experience in clinical research across a broad spectrum of medical specialties and therapeutic areas
• Monitors are regionally based, reducing travel time and the expense of site visits

DSP has a unique compensation structure for its Monitors, and we are proud of a very low turnover rate, creating greater study continuity, Monitor dependability, and fewer learning curves. At DSP, each Monitor is assigned fewer studies (maximum of 3 studies), and is therefore more involved in each study.

Our CRAs use state-of-the-art communications and management tools to provide timely and responsive communications, real time data and reporting, and centralized tracking and management of study data and milestones.

Site Monitoring Locations

• Overview
• Study Management
• TrialTrak
• Site Monitoring
• Investigator Site Management
• Data Management
• Therapeutic Experience
• Additional Services