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Job Description
Conducting site visits at medical institutions to ensure that trials are carried out in accordance with the study protocol.
Ensuring adherence to GCP (International Conference on Harmonisation - Good Clinical Practice) guidelines and other regulatory requirements.
Verifying the accuracy and completeness of collected trial data, and initiating necessary corrections or improvements.
Providing education and training for medical staff involved in the clinical study to ensure compliance with proper trial conduct.
Current Contingent Workers apply
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