IQVIA LLC is seeking a Clinical Research Associate (CRA) to join our team in the United States to support site monitoring, regulatory compliance, and data quality across trials.
You will monitor sites, collaborate with cross-functional teams, and contribute to patient safety and trial integrity in a fast-paced environment. A Bachelor’s degree and 1.5+ years of on-site monitoring experience are required.
#J-18808-LjbffrSenior CRA: Lead Site Monitoring & Trial Excellence in durham at Unknown Company
This position is listed as full time and onsite.