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“As a Clinical Operations Manager I act as a Clinical Trial Leader and coordinate the activities for each trial region in large international multi-center studies according to Good Clinical Practice (GCP).
My main task consists of coordinating the operational part of clinical studies. This includes activities like preparing the documentation for the regulatory authorities, selecting study centers, implementing the logistical part of the study (vaccine supply, laboratory material, etc.) and finding agreements with CROs (Contract Research Organizations), investigators, local and central laboratories.”
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