Clinical Research Associate/Coordinator I

What you’d do

Enrolls eligible patients in cancer clinical trials and manages data collection and submission for multiple studies. Acts as liaison between the clinical team, sponsor, and IRB, with a mix of data abstraction, regulatory work, and patient coordination. Full time. Found on the employer's careers page on Oct 20, 2026. Apply through the link.

You’ll need

• Working knowledge of clinical research protocols
• Ability to interpret acceptability of data results
• Careful attention to detail
• Organizational and communication skills
• Direct patient contact