Clinical Research Coordinator 2

What you’d do

Coordinate routine clinical study activities, including chart review and pre-screening for participant eligibility, data collection, scheduling study visits, and maintaining enrollment per protocol. Full time, with ability to work evenings, nights, and weekends as necessary. Found on the employer's careers page on Oct 8, 2026. Apply through the link.

You’ll need

• Experience in clinical research
• Data management or protocol implementation experience
• Attention to detail
• Ability to work evenings, nights, and weekends