This position assists investigators as a coordinator of complex clinical research studies, potentially managing multiple studies simultaneously. The coordinator acts as a liaison between 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, collaborating on manuscripts and grant proposals, and preparing protocol amendments. Additionally, the coordinator develops forms and questionnaires, writes instructional procedure manuals, stays updated on scientific literature, and manages study implementation, compliance, record-keeping, participant progress assessments, and adverse event reporting. The position also involves making critical decisions regarding participant inclusion and protocol adjustments, resolving management issues, serving as a liaison with funding agencies, and evaluating/interpreting 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