California Clinical Trials Data Coordinator

Job Summary

A company is looking for a Clinical Trials Data Coordinator to ensure data integrity for various research studies.

Key Responsibilities

• Ensure data integrity through 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, with relevant experience considered as a substitute
• At least two years of experience in oncology clinical trials
• Working knowledge of clinical trials and applicable regulations