The Clinical Research Nurse will facilitate 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.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree