Clinical Research Monitoring Specialist

Reading Source: WhatJobs
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IQVIA is seeking a Site Monitor to perform monitoring visits, manage site relationships and ensure study data quality in accordance with GCP, ICH and sponsor requirements.

The role involves coordinating recruitment plans, handling regulatory submissions, maintaining TMF/ISF, and collaborating with study teams. A Bachelor's degree and at least 1 year on-site monitoring experience are preferred; strong English communication and organizational skills are essential.

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