Data Entry Coordinator

About the Role

The Clinical Research Data Entry Coordinator supports clinical trials by ensuring accurate and timely data entry into electronic data capture (EDC) systems while maintaining regulatory compliance.

Responsibilities

• Enter and verify source data in EDC systems
• Review source documentation for consistency
• Manage data queries with sponsors or CROs
• Ensure adherence to GCP and ICH guidelines
• Assist with study documentation
• Conduct data quality reviews
• Collaborate with study teams to facilitate smooth data flow

Requirements

• Associate's or bachelor's degree in a health-related field
• Experience with EDC platforms and data management tools
• Attention to detail
• Knowledge of clinical trial protocols and regulatory standards
• Strong communication skills

Preferred Qualifications

• Prior clinical research experience
• Familiarity with medical terminology
• Query resolution skills

Skills

• Accuracy
• Time management
• Confidentiality
• Problem-solving
• Process improvement