Clinical Research Associate

The Clinical Research Associate will coordinate, conduct and evaluate research related activity for clinical research projects as assigned. The primary purpose of this position is to oversee the regulatory component of the clinical trials as well as screening, enrollment and retention of student participants, to coordinate study visits, ensure quality of data collected throughout the research study, and implement the procedures and activities of the assigned study protocols, according to all applicable regulations and regulatory compliance, under the direction of the Principal Investigator and the Director of Clinical Research.

The Clinical Research Associate will handle the start-up and maintenance of regulatory process of the clinical trial studies managed by the OCR. The primary purpose of this position is to oversee the regulatory component of the clinical trials activities of the assigned study protocols, according to all applicable regulation and regulatory compliance, under the director of the Principal Investigator and Director of Clinical Research.