Clinical Research Associate
CurrentI am am currently a CRA for Medpace. As a CRA, my responsibilities include the following: - Conduct site qualification, initiation, monitoring, and close-out visits according to ICH-GCP, Medpace/Sponsor SOPs, and applicable regulatory requirements.- Responsible for overall site management for assigned sites, including written and verbal communication and scheduling of monitoring visits. - Responsible for completion of visit reports, follow up letters, and maintenance ofstudy-related database.