Prepare sites for conducting the study Assist in the development of systems & detail of timelines for each study’s aims Assist in the development of standard operating procedures for study protocols Assist with the training of medical assistants and nurses with regard to study protocols Review & prepare correspondence with the NorthShore IRB (initial submission, protocol amendments, adverse events, yearly progress reports, etc) Maintain regulatory documents as per sponsor & IRB protocols Responsible for accountability & maintenance of study medications. This may include dispensing study meds to patient, coordinating storage & maintenance of drug with NorthShore pharmacy, maintaining drug accountability & compliance of drug as per study protocol Complete study activities as dictated by research protocols (including face to face and telephone assessments, medical records abstraction, etc.) Coordinate & schedule appointments for diagnostic tests & procedures associated w/study protocols
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Job Type
Full-time
Career Level
Entry Level