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; · schedule and conduct study visits; · collect and enter data; register subjects and study visits in OnCore; · perform Epic research billing review; · maintain an up to date regulatory
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submissions both local and central. *Prior experience with OnCore clinical trial management system, Florence electronic regulatory system *Prior experience using Epic EHR. *Prior experience using electronic
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experience with IRB submissions both local and central. *Prior experience with OnCore clinical trial management system, Florence electronic regulatory system *Prior experience using Epic EHR. *Prior experience
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