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The Multi-center CRA works under general supervision to maintain regulatory files and monitor data quality and data and protocol compliance across participating study sites. The CRA will be trained on the institutional and federal regulations governing clinical research. The position involves a high volume of regulatory document coordination and tracking and clinical data review. This position does not include any direct patient contact.
PRINCIPAL RESPONSIBILITIES INCLUDE:
The CRA will perform the following duties under general supervision by the Clinical Research Manager:
QUALIFICATIONS:
Education:
Skills and Competencies:
The Clinical Research Associate II should also possess:
WORK ENVIRONMENT:
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