Clinical Trials Data Coordinator

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