Clinical Trial Coordinator

What you’d do

Supports one or more clinical trials, handling day-to-day administrative project activities and ensuring work follows the trial protocol, good clinical practice, and regulatory and sponsor standards. Full time in Boston. Found on the employer's careers page on Oct 15, 2026. Apply through the link.

You’ll need

• 1-2 years research related experience
• Familiarity with EDC and CTMS systems preferred
• Excellent organizational skills
• Strong written and verbal communication skills
• Ability to work autonomously