This position assists investigators as a coordinator of complex clinical research studies, potentially managing multiple studies simultaneously. The coordinator acts as a liaison with the school, sponsoring agency, community, and study participants. Key responsibilities include managing and recording all phases of study protocol to ensure compliance with sponsoring agency requirements. The role involves developing research project plans, interpreting results, preparing manuscripts and grant proposals, and assisting with protocol amendments. The coordinator will also develop forms and questionnaires, write instructional procedure manuals, and stay updated on scientific literature. Furthermore, the position requires implementing and managing study protocols, ensuring regulatory compliance, establishing record-keeping systems, assessing participant progress, analyzing and reporting adverse events, and making critical decisions regarding participant inclusion and protocol adjustments. The coordinator will resolve protocol management issues, recommend corrective actions, serve as a liaison with funding agencies, and evaluate and interpret clinical data to prepare presentations and reports.
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Job Type
Full-time
Career Level
Mid Level
Number of Employees
1,001-5,000 employees