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Job description
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.
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Worksite address
durham, NC, 27703, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.