Clinical Research Associate
The Clinical Research Associate module is designed to provide prospects activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs, and study protocols. Reviews regulatory documents as required and prepare site visit reports. Responsible for multiple projects and must work both independently and in a team environment. May participate in the study development and start up process including; reviewing protocols, designing and/or reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings, working with management on monitoring strategy, and/or developing project-specific CRA training. Would participate in clinical training programs and maintain awareness of developments in the field of clinical research
