Works under limited supervision and oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP). Performs research activities supporting clinical trials, including data entry, query and inventory management, biospecimen processing and storage, biospecimen shipment, and clerical duties to help investigators organize, gather, and compile clinical research data. Organizes and maintains documentation required for clinical trials. May provide technical support to help ensure adherence to research protocols and the quality of information received.
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Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED