The primary responsibility of the Clinical Research Associate I (CRA I) is support of the research team in the conduct of department research projects. Responsibilities include but are not limited to the following\: Perform study startup, implementation, and closeout activities Assist research team with coordination and entry of research data Assist with regulatory submissions to the Institutional Review Board, and maintain compliance with all federal and local agencies in accordance with Good Clinical Practice guidelines Interact with patients and families for securing informed consent, scheduling research visits, and collection of data Maintain documentation for regulatory binder, adverse event reporting, and communications between sponsors and sites Other special skills specific to assigned research area may include phlebotomy, sample collection, processing or shipping, ECGs, chart abstraction or other duties as assigned Manage personal career development and administrative tasks
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Job Type
Full-time
Career Level
Entry Level