Clinical Research Nurse II
US-NJ-Camden
External Career Portal
Req #: 80453
Type: Full Time
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Responsibilities: * Facilitates preparation of IRB protocol submissions and informed consent forms. * Key individual in identifying, recruiting and interacting with patients throughout the entire * study. * Responsible for completing and maintaining all study documents, in compliance with IRB, * Cooper Health System, sponsor and FDA requirements. #LI-CU1 Qualifications: Advanced understanding of Microsoft Office.
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