California Licensed Clinical Trials 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 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 as a substitute
• At least two years of experience in oncology clinical trials
• Working knowledge of clinical trials and relevant regulations
• Familiarity with Good Clinical Practices (GCP) and HIPAA regulations
• Understanding of IRB requirements