Coordinate administrative and clinical aspects of multiple research projects. Collaborate with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols. Monitor and report on progress of projects. Assist with the recruitment, selection, scheduling, and monitoring of research project participants. Manage the handling of adverse events, compliance and other participant-related issues. Coordinate the preparation and delivery of departmental communications, presentations and marketing/educational materials. Collaborate to ensure compliance with applicable regulations and standards. Assist with responding to and preparing for audits. Coordinate activities for the Institutional Review Board (IRB). Prepare and maintain documents, presentations, files, training materials and databases needed for IRB compliance.
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Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED