Operational responsibility to set-up the local Trial Master File (eTMF) and Investigator Site File including tracking of documents. Maintain and close the local TMF (in electronic or paper form depending on study) ensuring International Conference of Harmonisation Guidelines for Good Clinical Practice (ICH/GCP) compliance and local requirements. Support the CRA in the maintenance and close out activities for the ISF.
https://www.indeed.com/viewjob?t=clinical+trial+management+specialist&jk=55e0df1f86de6f8d&_ga=2.87464216.1878940423.1544377302-2077807285.1533320279
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