Clinical Trials Data Coordinator

Job Summary

A company is looking for a Clinical Trials Data Coordinator.

Key Responsibilities:

• Ensure data integrity for research studies by completing data abstraction, CRF completion, and query resolution
• Coordinate sponsor monitor visits and maintain audit-ready data
• Oversee electronic research records and patient information in the CTMS

Required Qualifications:

• Bachelor's Degree or relevant experience in lieu of a degree
• At least two years of experience in oncology clinical trials
• Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements