Research Study Coordinator- PRN bei Gastroenterology Associates of the Piedmont

Description

The Clinical Research Coordinator is responsible for carrying out all research activities per individual study protocol(s) assigned, while remaining compliant with regulatory guidelines as required by Sponsor, FDA, and IRB. The Clinical Research Coordinator ensures all documentation is true, accurate, and complete for each study activity performed. This is a PRN position. 

Requirements

The Clinical Research Coordinator must have knowledge of clinical trial documentation requirements, familiarity with healthcare systems, regulations, policies and functions. He/ she must also have knowledge of Clinical Trial Agreements,  study start up processes, close out processes, and knowledge of customer service principles and techniques.