The CRA (Clinical Research Associate),also called clinical monitor, is a health-care professional who performs many activities related to clinical trials. The CRA's task is to check and ensure data quality and regulations, including the Helsinki Declaration, implementation of Good Clinical Practice (GCP) and compliance with the study protocol. Monitoring can significantly improve data quality in clinical studies. But what is a CRA doing on a normal day? Find out some answers in this interview with Dr. Andreas Grund and CRA Bianca Seifert!

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