Data Entry Coordinator

Description

• Verify source documents using the 'buddy check' method.
• Assist in preparing for internal and external data audits with clinical operations, quality, and regulatory teams.
• Maintain professional relationships with Clinical Operations, Quality, Regulatory, CROs, Sponsors, and key clinical trial personnel.
• Accurately and efficiently transcribe data from source documents to electronic data capture systems.
• Assist CRCs in entering data from paper source documents to eCRFs correctly, accurately, and promptly for multiple clinical trials.
• Ensure timely data entry through department and study tracking.
• Support and ensure strict adherence to best practices, FDA Code of Federal Regulations, ICH, GCP, standard operating procedures, site working practices, protocol, and company guidelines and policies.

Requirements

• Complete training and obtain applicable certificates and access to CRFs/EDC.
• Excellent computer skills and knowledge of medical/research terminology.
• Detail-oriented and meticulous approach to data entry.
• Self-directed and able to work with minimal supervision.
• Minimum high school graduate or equivalent.
• Proficiency in electronic data capture (EDC) systems.
• One year of data entry or related experience preferred.
• Motivated to work consistently in a fast-paced and rapidly changing environment.
• Ability to identify and correct mistakes in data due to familiarity with healthcare.
• Ability to manage multiple projects and responsibilities.
• Experience in data entry, preferably with some healthcare experience.

Benefits

Training + Development

Interview process

Visa Sponsorship

Security clearance