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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

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

Clinical Trials Data Coordinator

Clinical Trials Data Coordinator

Behavioral Health Market Context

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