Collects & organizes patient data- Maintains records and databases- Uses software programs to generate graphs and reports- Assists with recruiting patients for clinical trials- Obtains patient study data from medical records, physicians, etc.- Conducts library searches- Verifies accuracy of study forms- Updates study forms per protocol- Documents patient visits and procedures- Assists with regulatory binders and QA/QC procedures- Assists with interviewing study subjects- Administers and scores questionnaires- Provides basic explanation of study and in some cases obtains informed consent from subjects- Performs study procedures, which may include phlebotomy.- He or she will be responsible for patient scheduling and recruitment as well as all subject-oriented study procedures, such as administration of psychiatric scales and neuropsychological testing protocols, careful monitoring of adverse events, administrative duties related to the careful operation of study protocol, and database management and quality assurance PRINCIPAL DUTIES AND RESPONSIBILITIES: Please note, the functions below are representative of major duties that are typically associated with these positions.