Short Description: 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.
Special Requirements: Education:Graduate from an accredited RN program.Experience:0-5 years clinical research experience. Required License/Certifications/ Registration:NJ-RN License, CRC/CRCC preferred.Other Qualifications:Advanced understanding of Microsoft Office. Scheduled Days / Hours: M-F 8 - 4:30; License (or Certification):NJ-RN Required