Clinical Trials Administrator
Coordinates and organizes clinical studies and/or trials. Drafts and/or evaluates protocols, policies and procedures regarding research projects and studies. Maintains pertinent records and documentation. May follow research participants or patients from recruitment through treatment, discharge and follow-up. May be responsible for collecting, recording, and preparing data for publication. Coordinates with the Office of Grants and Contract Administration and Institutional Review Board. May perform general nursing/clinical duties.
Coordinates and performs a variety of research and administrative activities required in the management of clinical trials research. Duties include assisting principal investigators and/or other members of the research team in the development of protocols, budgets, and plans for clinical research studies; coordinating the preparation and submission of reports. Assists with grant writing and IRBs. Serves as a resources for technicians and other researchers. Performs other duties as assigned.
Expected annual salary range:
$47,486.40 - $74,484.80
Bachelor's degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement.