Position will be directly responsible for facilitating and coordinating the daily clinical trial activities for multiple clinical trials, working closely with investigators, research sponsors, contract research organization representatives, research staff, and UAMS institutional oversight offices. Position must be able to organize complex projects, provide attention to detail, and communicate effectively. Will apply knowledge of local policies, federal regulations and guidelines in support of an assigned clinical trial portfolio and the objectives of the TRI CTIU. Contributes information and ideas related to areas of responsibility as part of a cross functional team. Ensures effective and efficient workflow and adherence to quality standards for staff/program and self. Position maintains a working knowledge of the Code of Federal Regulations and the code of conduct for human research.
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Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED