Clinical Research Coordinator

The Clinical Research Coordinator is responsible for overseeing data management activities, protocol management activities, and regulatory compliance with federal and local regulations as they relate to the conduct of clinical trials. This role ensures adherence to Good Clinical Practice (GCP) and Institutional Policies while coordinating with Principal Investigators, Sponsor Representatives, and site staff.

Requirements

• Bachelor's degree in a related field
• 0-2 years of experience in clinical research