Works under limited supervision and oversees the day-to-day activities of multiple research studies with quantitative and qualitative methods in accordance with Good Clinical Research Practice (GCP). Performs a variety of research activities in support of research (including database management, and clerical duties to assist investigators in organizing, gathering, and compiling clinical research data. Recruits, assists with consenting subjects, and conducts study visits. Clinical or research experience with people who use substances is preferred. Essential Functions: Interacts with co-workers, visitors, and other staff consistent with the values of Jefferson. Performs a variety of research, database, and clerical duties in support of research studies to assist investigators in organizing, gathering and compiling clinical research data. Organizes and maintains documentation required for clinical trial(s). Informs Principal Investigator and/or designated individual on any issues concerning patients' response to research questions Assists the Principal Investigator with regulatory requirements including IRB submissions. May assist in the enrollment of human subjects. May provide clerical and technical support to ensure adherence to research protocols and quality of information received. Assists with qualitative interviews and coding and administering surveys 100% IN-PERSON Scheduled shift hours will be 8am-5pm
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Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED