Clinical Research Coordinator II-Hosp & RI Factor Program

What you’d do

Manages clinical study elements to meet protocol obligations under ICH/GCP guidelines, coordinating start-up, launch, day-to-day management, and closure activities. Also trains and mentors other CRCs. Full time. Found on the employer's careers page on Oct 7, 2026. Apply through the link.

You’ll need

• Associate's degree or equivalent work experience
• Understanding of medical terminology and clinical trials
• Working knowledge of PCs and data management software
• CRA/CRC certification preferred