Clinical Research Coordinator

Job Summary

A company is looking for a Clinical Research Coordinator to support early-phase oncology trials.

Key Responsibilities

• Communicate with study sponsors and staff regarding protocol status and concerns
• Monitor study conduct to ensure compliance with protocols and Good Clinical Practice
• Assist with patient screening, eligibility determination, and the informed consent process

Required Qualifications, Training, and Education

• High School Diploma or GED
• 2 years of clinical research experience
• Basic understanding of oncology clinical trials, particularly Phase 1 studies
• Working knowledge of GCP and regulatory requirements
• Proficient in Microsoft Office Suite and clinical trial management software