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 the conduct of oncology clinical trials
• Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements
• In-depth knowledge of Good Clinical Practices (GCP), FDA regulations, NIH guidelines, and HIPAA regulations