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 oncology clinical trials Working knowledge of clinical trials and relevant regulations In-depth knowledge of Good Clinical Practices (GCP) and FDA regulations Understanding of NIH guidelines and HIPAA regulations