Clinical Research Coordinator

The Clinical Research Coordinator manages the daily operations of clinical trials, ensuring that innovative treatment modalities are executed with uncompromising ethical standards. You will act as a liaison between distinguished experts in psychiatry and the human subjects participating in our studies.

• Study Oversight: Coordinate the implementation of research protocols for studies such as those focusing on Treatment-Resistant Depression and Early Intervention in Psychosis.
• Ethical Compliance: Ensure all research activities adhere to the safety and privacy standards set by our Institutional Review Board (IRB) and the Local Review Research Committee (LRRC).
• Regulatory Documentation: Manage Federal Financial Conflict of Interest (FCOI) disclosures and ensure all investigators are current with mandatory four-year retraining cycles.
• Patient Advocacy: Facilitate informed consent processes, ensuring participants receive comprehensive data regarding study goals and potential risks.