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IQVIA is seeking a Clinical Research Associate to monitor study sites and ensure data are collected per protocol and regulatory requirements. This on-site role supports site selection, initiation, monitoring, and close-out visits across studies.
You will coordinate with site staff, manage recruitment plans, train sites, and maintain documentation in the TMF/ISF while upholding GCP and ICH guidelines. Proficiency with EDC/CTMS systems is preferred.
IQVIA is seeking a Clinical Research Associate to monitor study sites and ensure data are collected per protocol and regulatory requirements. This on-site role supports site selection, initiation, monitoring, and close-out visits across studies.
You will coordinate with site staff, manage recruitment plans, train sites, and maintain documentation in the TMF/ISF while upholding GCP and ICH guidelines. Proficiency with EDC/CTMS systems is preferred.