The Research Coordinator I will assist investigators and the research team with the planning and implementation of oncology clinical trials. Duties include subject recruitment and consent, research procedures as appropriate, case report form (CRF) completion, communication and meetings with sponsor representatives, scheduling and assisting with clinical trial monitoring activities, research billing reviews, IRB submissions, and reporting adverse events and protocol deviations.
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Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED