Clinical Trials Coordinator

What you’d do

Coordinates care for patients and families enrolled in clinical research trials, handling communication, regulatory, and research tasks. Summarizes study accrual and toxicity data and liaises between the Data and Safety Monitoring Board and Principal Investigators. Full time. Found on the employer's careers page on Oct 12, 2026. Apply through the link.

You’ll need

• 3 years of clinical experience
• Knowledge of clinical study conduct and research principles
• Master's degree in Business Administration, Healthcare Administration, or a scientific field
• Experience creating and negotiating study budgets and contracts