Texas Licensed Clinical Research Coordinator

Job Summary

A company is looking for a Clinical Research Coordinator, RN who will support the daily activities of early phase oncology clinical trials.

Key Responsibilities

• Monitor the day-to-day conduct of assigned studies in accordance with protocol requirements and Good Clinical Practice
• Facilitate the informed consent process and assist with patient screening and eligibility determination
• Communicate regularly with study sponsors and staff regarding protocol status and compliance

Required Qualifications

• Associate's degree in Nursing
• RN license in the state of practice
• 2 years of clinical research experience
• Basic understanding of oncology clinical trials, particularly Phase 1 studies
• Working knowledge of Good Clinical Practice and regulatory requirements