Clinical Research Coordinator I

What you’d do

Coordinates phase I, II, and III oncology clinical trials for the Lombardi Comprehensive Cancer Center, handling informed consent, study scheduling, specimen collection, and patient communication. Full time. Found on the employer's careers page on Oct 6, 2026. Apply through the link.

You’ll need

• Bachelor's in a scientific or health related field
• 3–5 years related clinical research experience preferred
• Informed consent and GCP knowledge
• Strong attention to detail
• Ability to prioritize competing responsibilities