Clinical Trial Research Coordinator II

What you’d do

Coordinates day-to-day activities of research protocols, assesses and determines patient eligibility for studies, and ensures accurate data collection, documentation, and participant safety. Includes recruiting research subjects and general administrative duties supporting the study. Full time. Found on the employer's careers page on Oct 21, 2026. Apply through the link.

You’ll need

• Bachelor's degree
• Four years of research experience
• CCRC (ACRP) or CCRP (SOCRA) certification
• Clinical research subject recruitment
• Data collection and documentation