Clinical Research Coordinator - Union, SC
IQVIA · Union, SC
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Role summary
This on-site, part-time role (24 hours/week) supports clinical research studies in Union, SC, involving clinical procedures, patient recruitment, data collection, and GCP compliance. The coordinator works under principal investigator supervision to ensure protocol adherence and data quality. A bachelor's degree and minimum one year of clinical research experience are required.
Privacy & handoff
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