Clinical Research Data Entry Coordinator

Responsibilities

• •Records collected subject data promptly and efficiently into study data system while maintaining HIPAA compliance
• •Review study database regularly
• •Reviews subject charts for completeness and accuracy while entering subject data
• •Ensure all corrections made by study coordinator in subject chart are legible and compliant with GCP guidelines
• •Observe, assist, collect and record all necessary data for follow up
• •Report instances of chart incompleteness and inconsistencies
• •Transcribe subject study information from source document
• •4 more items(s)