Clinical Research Associate: Site Monitoring & Data Quality
Listed on 2026-10-13
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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.
Step into the Clinical Research Associate:
Site Monitoring & Data Quality role at IQVIA in Durham, NC, United States and grow with us.
We would love to welcome a new Clinical Research Associate:
Site Monitoring & Data Quality to our group in Durham, NC, United States.
For the Clinical Research Associate:
Site Monitoring & Data Quality position at IQVIA, we are reviewing applications now.
Please review the full job details above before applying.
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