The Clinical Research Coordinator II handles administrative activities associated with clinical trials, including managing research project databases, developing study documents, and conducting screenings for study participants. The position requires experience in clinical research and may involve patient contact and handling of potentially infectious materials.
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