Oversees implementation of research projects, including screening participants, ensuring appropriate scheduling and follow-up for research participants, and coordinating with other staff and volunteers involved in the research projects. Schedules and runs participants in clinical research protocols; involves obtaining informed consent, administering questionnaires, performing interventions and conducting diagnostic and testing protocols. Manages data; includes developing online data management systems, maintaining subject charts and scanning paper forms and upload them to the central database. Ensure that all paper and computer files are maintained in a confidential manner. Maintains effective written and verbal communication with PIs and other lab members and participates actively in lab meetings. Trains other research and volunteer research assistants in data collection and data management; ensures their compliance with IRB and privacy policies.
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Job Type
Full-time
Career Level
Mid Level