Clinical Research Coordinator 2

What you’d do

Coordinate clinical research studies from protocol initiation to close-out, handling day-to-day operations, participant safety, regulatory compliance, and study administration. Full time, with evenings, nights, and weekends as necessary. Found on the employer's careers page on Oct 7, 2026. Apply through the link.

You’ll need

• Mid-level clinical research experience
• Knowledge of regulatory and sponsor guidelines
• Attention to detail and accuracy
• Ability to work evenings, nights, and weekends
• Discretion with confidential information