Clinical Trials Data Coordinator

Job Summary

A company is looking for a Clinical Trials Data Coordinator.

Key Responsibilities

• Ensure data integrity for various research studies through data abstraction and CRF completion
• Coordinate sponsor monitor visits and maintain audit-ready data
• Oversee electronic research records and patient information in the CTMS

Required Qualifications

• Bachelor's Degree, with relevant experience as a substitute
• At least two years of experience related to oncology clinical trials
• Working knowledge of clinical trials and relevant regulations
• In-depth knowledge of Good Clinical Practices (GCP) and FDA regulations
• Understanding of NIH guidelines and HIPAA regulations