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 that support clinical trials, including database management, biological specimen collection and processing, and clerical duties, helping investigators organize, gather, and compile clinical research data. Recruits participants, assists with informed consent, and conducts study visits. The role also supports trial documentation, regulatory filings, and adherence to research protocols and data quality requirements.
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Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED