Clinical Research Coordinator

What you’d do

Oversees day-to-day clinical trial activities under Good Clinical Practice, managing studies from startup through closeout. Coordinates patient screening, recruitment, enrollment, and informed consent, and maintains regulatory and IRB documentation. Full time. Found on the employer's careers page on Oct 12, 2026. Apply through the link.

You’ll need

• High School Diploma with 6 years clinical research experience, OR
• Bachelor's degree with 2 years clinical research experience, OR
• Master's degree with 1 year clinical research experience
• Knowledge of Good Clinical Practice (GCP) guidelines
• Experience with IRB and regulatory documentation