Under supervision of the Clinical Study Manager, the Clinical Trial Intern (CTI) is responsible for administrative activities in support of ongoing, Cyberonics clinical trials. This may include review and audit of in-house, clinical study file documentation, logging and tracking shipping of clinical trial documents and materials, filing clinical trials documentation including electronic scanning, electronic and hard-copy filing of clinical research documents, and drafting letters and e-mails to clinical study sites. PRIMARY ACTIVITIES Under supervision, CTIs review and audit in-house, clinical study file documentation Maintains clinical study files including creation and daily upkeep File clinical trials documentation including scanning documents for electronic copies, filing hard copies in clinical study files, and maintaining records of documents filed Log and track shipping of clinical trial documents and materials Assist in preparation and assembly of mass mailings to clinical study sites Perform other duties as required by supervisor MINIMUM REQUIREMENTS AND QUALIFICATIONS Attention to detail Good organizational skills Proficient in both verbal and written communication skills Familiar with filing and organizing DESIRED SKILLS AND QUALIFICATIONS High school diploma and current undergraduate or college or nursing graduate with interest in clinical research field

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Intern, Clinical Trials

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