Assists in study start up; collection and review of regulatory documents• Provides support to clinicians in preparing materials for assessments/treatment sessions and coordinates study visits• Administratively and clinically manage an average of six to eight clinical trials• Recruits participants, evaluates eligibility, and assists in collecting data.• Prepares and submits IRB required documents• Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials. Collects documents needed to initiate the study and submit to the sponsor (e.g., FDA Forms 1572, CVs, etc.)• Performs needed procedures for protocol defined research/clinic visits. Takes vital signs, weight, height measurements and records in patient's chart (or source doc) and in summary reports and documents• Dispenses study medication in a professional and accountable manner following protocol requirements• Adheres to Good Clinical Practices and study protocols• Schedules monitor visits and set up for monitoring visits prior to monitor’s arrival