California Licensed Clinical Data Coordinator

Job Summary

Ensuring data integrity for various research studies, the full-time remote California Licensed Clinical Data Coordinator will manage data abstraction, CRF completion, query resolution, and sponsor monitor visit coordination while maintaining audit-ready data.

Key responsibilities

• Oversee electronic research records and patient information in the CTMS
• Communicate protocol deviations or issues related to study execution effectively
• Maintain strict adherence to study protocols and ensure proper execution of study parameters

Required qualifications

• Bachelor's Degree, with relevant experience potentially substituting for the degree
• 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