Clinical Research Associate: Site Monitoring & Data Quality
Listed on 2026-10-06
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Research/Development
Research Assistant/Associate, Clinical Research
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.
We invite applications for the Clinical Research Associate:
Site Monitoring & Data Quality position located in Durham, NC, United States.
As a Clinical Research Associate:
Site Monitoring & Data Quality, you will play an important part at IQVIA Argentina in Durham, NC, United States.
The following opportunity is for a Clinical Research Associate:
Site Monitoring & Data Quality with IQVIA Argentina.
Our organisation is growing, and we are hiring a Clinical Research Associate:
Site Monitoring & Data Quality in Durham, NC, United States.
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