Address
Form of workLocation: New Orleans, LA
SummaryThe Clinical Research Coordinator II will coordinate and conduct the day-to-day operations of TRIAD ongoing studies in cardiovascular diseases. 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 the primary resource for protocols, the Clinical Research Coordinator acts as a liaison between the patient, investigator, Institutional Review Board and sponsor. The Clinical Research Coordinator II screens, enrolls and follows study patients, ensuring protocol compliance, and effective monitoring of clinical trial subjects. The Clinical Research Coordinator II is also responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files.
Required Qualifications•Bachelor’s Degree in public health or other science area or RN with current state licensure at the time of hire and one (1) year of related work experienceOR•LPN with current state licensure at the time of hire and four (4) years of related work experience; OR•Master’s Degree in a related field
Preferred Qualifications•Knowledge of IRB submission process and requirements.•Knowledge of good clinical practices as set forth by federal regulations.
