This position typically reports to the Principal Investigator, Clinical Research Manager, or a Lead Clinical Research Coordinator. Working under general supervision, the Clinical Research Coordinator II is responsible for the coordination of more complex clinical research related activities, including but not limited to maintenance of regulatory documents, screening and enrolling patients, collecting biospecimens, performing clinical tasks as appropriately trained and delegated, data collection and entry, coordinating study and monitoring visits, and submitting reports as needed. Work at this level meets the FLSA criteria for a professional exemption since the primary duties are directly related to the clinical studies operations, requiring advanced knowledge and the application of discretion and independent judgment on matters of significance with respect to clinical study protocols, quality data and coordination of operational activities. This position differs from the Clinical Research Coordinator I classification by providing independent coordination of multiple, complex clinical research studies.
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Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed