The Clinical Research Coordinator II handles administrative activities associated with the conduct of clinical trials, including managing research project databases, developing study documents, and ensuring compliance with research protocols.
Requirements
- High School Diploma or GED and five years of clinical research experience
- Two years of college in a scientific, health related, or business administration program and three years clinical research experience
- Licensed as a practical nurse (LPN) and two years clinical research experience
- Bachelor's degree in a scientific, health related, or business administration related program and one year of clinical research experience
- Master's degree, MD or PhD in a scientific, health related or business administration program