Data Entry Coordinator

About the Role

The Data Entry Coordinator I is responsible for accurately transcribing clinical research data from source documents to electronic data capture systems, adhering to ALCOA-C principles.

Responsibilities

• Ensure timely data entry and maintain professional relationships with clinical trial personnel.
• Assist in preparing for data audits and verify source documents.
• Support compliance with GCP, FDA CFR, ICH guidelines, and company SOPs.
• Help Clinical Research Coordinators (CRCs) with data entry from paper to electronic case report forms (eCRFs).
• Complete required training and obtain necessary certifications.
• Perform other duties as assigned.

Requirements

• High school diploma or equivalent; experience in data entry preferred.
• Excellent computer skills and understanding of medical/research terminology.
• Self-motivated, detail-oriented, and able to work independently.
• Strong verbal and written communication skills.
• Ability to manage multiple projects in a fast-paced environment.

Working Conditions

Office environment with physical requirements including sitting, standing, walking, and occasional lifting up to 20 pounds. On-site work with scheduled reporting is required.