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.
0-5 years clinical research experience.
BSN required.
NJ-RN License, CRC/CRCC preferred.
USD $34.00 - USD $56.00
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