Clinical Research Coordinator 3

What you’d do

Manage daily operations of multiple clinical research studies, from protocol development through close-out, ensuring regulatory compliance and participant safety. Mentor less experienced coordinators. Full time. Found on the employer's careers page on Oct 8, 2026. Apply through the link.

You’ll need

• Experience coordinating clinical research protocols
• Knowledge of regulatory and sponsor guidelines
• Ability to manage multiple studies
• Mentoring experience
• Technical proficiency with office software