The primary responsibility of the Clinical Research Coordinator II is to manage all aspects of conducting clinical trials. The Clinical Research Coordinator II is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth 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 Research Coordinator II is able to screen, enroll and follow study patients, under supervision, ensuring protocol compliance and close patient monitoring, continuing the required learning process record in this second level position for advancement towards a Clinical Research Coordinator III position. The Clinical Research Coordinator is responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files, under direct supervision. Minimum Qualification: Bachelor's degree or RN with current Louisiana state licensure at the time of hire and one (1) year of related work experience OR LPN with current Louisiana state licensure at the time of hire and four (4) years of related work experience Preferred Qualification: Knowledge of IRB submission process and requirements Knowledge of good clinical practices as set forth by federal regulations