Clinical Research Coordinator
Research Department – Full-time/Study focus area: Interventional (IV)
The primary responsibility of the Clinical Research Coordinator (CRC) is to manage all aspects of conducting clinical trials. The CRC is required to have an in-depth knowledge of protocol requirements and good clinical practice as set forth by federal regulations. The CRC will act as liaison between the investigators, primary care providers, the institutional review board (IRB), and the sponsor. Along with the investigator, the CRC will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while subjects are on study. The CRC is responsible for all data and source documentation, adverse event reporting, and maintenance of complete regulatory files.
Bachelor’s degree or equivalent experience required. A minimum of two years clinical experience required, cardiology experience preferred (electrophysiology or cath lab experience highly desired) and two to four years research experience desired. Valid Minnesota RN license preferred.
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POSTED: June 27, 2014