The primary responsibility of theClinical Research Coordinator II is to manage all aspects of conductingclinical trials. The Clinical Research Coordinator II is required to have anin-depth knowledge of protocol requirements and good clinical practices as setforth by federal regulations. As one of the primary resources for the protocol,the Clinical Research Coordinator II acts as a liaison between the patient,investigator, Institutional Review Board and sponsor. The Clinical ResearchCoordinator II is able to screen, enroll and follow study patients, undersupervision, ensuring protocol compliance and close patient monitoring,continuing the required learning process record in this second level positionfor advancement towards a Clinical Research Coordinator III position. TheClinical Research Coordinator II is responsible for all data and sourcedocumentation, adverse event reporting and maintenance of complete regulatoryfiles, under direct supervision.