IQVIA is seeking a Site Monitor to ensure study sites conduct and report data per protocol, GCP, and sponsor requirements. You will perform monitoring visits, validate site activities, and manage regulatory submissions.
Strong communication and organization are essential for coordinating with sites and internal teams. The role emphasizes on-site monitoring, data integrity, and documentation, with potential involvement in site recruitment planning and startup activities.
#J-18808-LjbffrClinical Research Associate: Site Monitoring & Data Quality in durham at Unknown Company
This position is listed as full time and onsite.