Clinical Research Assistant - Centerville, OH
trial management system (CTMS) Preparing and maintaining study files, and timely submission of information Collecting, submitting and assisting in maintaining relevant regulatory and ethics documents...
Clinical Research Associate II
An equivalent amount of experience can be substituted as appropriate Minimum of at least 1 year of Onsite Clinical Monitoring experience along with at least 1 year total in clinical research experience...
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...
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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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