Works under limited supervision and oversees the day-to-day activities of clinical trials in accordance with Good Clinical Research Practice (GCP). Performs research activities to support trials, including database management, biological specimen collection and processing, and clerical duties. Assists investigators with organizing, gathering, and compiling clinical research data; recruits and assists with consenting subjects; and conducts study visits.
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Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED