ICON seeks a Clinical Research Associate II to conduct clinical trial monitoring activities in Georgia, including site qualification, protocol compliance oversight, and data integrity management. The role involves travel and collaboration with investigators to support efficient study operations.
Responsibilities
Requirements
...managing multiple priorities. \n Administer business applications and time-sensitive processes including AP, CETS, CTS, ESC, ERT, FFP, Kronos/SAP Masterfiles, and Respond & Recover. \n Create customized reports using Excel Pivot Tables, advanced formulas, and macros. \n...
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