Clinical Research Coordinator II-Psychiatry Addiction Institute Dr. Hurd

Job description

Under minimal supervision, coordinates the clinical assessments of the study subjects; analyzes and assists in interpreting moderately complex clinical research data. Prepares grant applications and documents and assists in protocol submissions (for e.g., Institutional Review Board, Grants and Contracts Office). - Analyzes moderately complex clinical research data; Assists in interpreting clinical research data. - Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects. - Prepares and ensures grant applications, IRB/GCO documents are submitted. - Ensures accurate and complete compilation of subject data through chart reviews. - Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials. - Obtains informed consent under supervision of the Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects, and for studies involving genetic tests. - Independently obtains informed consent for other clinical studies. - Mentors Clinical Rese...