Clinical Research Associate/Coordinator I

What you’d do

Screen patients for cancer study eligibility, obtain informed consent, and manage data collection and IRB reporting as liaison between clinical team and sponsors. Full-time role with direct patient contact, working under the Clinical Research Manager. Found on the employer's careers page on Oct 8, 2026. Apply through the link.

You’ll need

• Working knowledge of clinical research protocols
• Ability to obtain informed consent
• Data abstraction and entry skills
• Attention to detail
• Full-time availability