Key Responsibilities
Our system performs a wide range of CRA duties, encompassing site selection and initiation, routine monitoring visits, and close-out visits.
Site Selection and Initiation
* Identify potential sites for clinical trials
* Ensure sites meet study requirements
Routine Monitoring Visits
* Conduct regular on-site inspections
* Evaluate study progress and data quality
Closing Out Sites
* Complete final visit procedures
* Lock databases to ensure data integrity