Clinical Trial Management System, CTMS). Perform QC check of reports generated from CTMS system where required....
Sr Clinical Research Associate I
As a PPD CRA, you will perform and coordinate all aspects of the clinical monitoring and site management process....
Remote WorkSenior Clinical Research Associate, Internal Medicine, Homebased, Us - Iqvia Biotechnology
Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research....
Senior Clinical Research Associate I
An equivalent amount of experience can be substituted as appropriate Minimum of at least 2 years of onsite Clinical Monitoring experience Advanced site monitoring; study site management; and registry...
Senior Clinical Research Associate II, FSP
Monitoring experience Valid Driver's License Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries Thorough understanding of the...
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Everything we do in healthcare has to be discovered and thoroughly tested before it can be put into practice. In this course, you will explore clinical research its challenges and its huge...
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