Clinical Research Associate II

What you’d do

Coordinate clinical research studies: recruit and screen participants, obtain informed consent, collect data, and keep protocols on track. Handle IRB submissions, budgets, sponsor communication, and train support staff. Full time. Found on the employer's careers page on Oct 19, 2026. Apply through the link.

You’ll need

• Strong project management and organization
• Excellent verbal and written communication
• High attention to detail
• IRB submission experience
• Participant recruitment and informed consent