The Clinical Research Assistant B directs the activities of workers engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives. This role may involve evaluating and analyzing clinical data. The assistant is responsible for aiding with study coordination and recruitment for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects within a specific division. They work directly with study physicians, research coordinators, project managers, and other research staff. Key tasks include performing screening visits, consenting participants, processing and shipping laboratory samples, entering data into databases, and escorting participants to other testing/procedure areas. Additionally, the position requires scheduling subjects for appointments, procedures, or inpatient stays as dictated by study protocols, performing specific protocol procedures such as interviewing subjects, taking vital signs, and conducting electrocardiograms. The assistant will also assess the eligibility of potential subjects through methods like screening interviews, medical record reviews, or discussions with physicians and nurses, prepare study-related documentation (e.g., protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, progress reports), and inform patients or caregivers about study aspects and expected outcomes.
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Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
Number of Employees
11-50 employees