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OhioHealth
Overview
Coordinates clinical research studies in collaboration with the Principal Investigator, ensuring adherence to GCP guidelines and federal regulations. Manages day-to-day activities including participant recruitment, informed consent, data collection, and regulatory reporting.
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Compensation
Salary not listed
Posted
3 days ago
Provides coordination and administrative support for clinical trials, including data entry, specimen processing, and regulatory documentation. Assists research staff with IRB submissions, patient screening, and maintaining study records to ensure operational efficiency.
6 days ago
