The Clinical Research Associate (CRA) participates in the preparation and execution of pre-market to post-market clinical investigations, overseeing the progress of clinical investigations by conducting site qualification, initiation, interim monitoring and close out visits to clinical sites and monitoring clinical investigations in accordance with Good Clinical Practice/ISO 14155, and procedures set forth by RQM+ and sponsors.
Job listings
The Clinical Research Associate I (CRA I) primarily oversees the progress of clinical investigations by conducting site interim monitoring visits to clinical sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by RQM+ and sponsors. Works closely with the Clinical Trial Manager (CTM) and/or Lead CRA to ensure all monitoring activities are conducted according to study requirements.