Clinical Data Entry Coordinator

About the role

The Clinical Data Entry Coordinator will support oncology clinical trials by accurately collecting, transcribing, and transmitting patient data from both paper and electronic case report forms (CRFs). This position ensures data integrity, facilitates regulatory compliance, and contributes directly to the development of innovative cancer therapies.

Key responsibilities

• Collect, transcribe, and transmit clinical data from paper and electronic CRFs for assigned investigational drug studies.
• Enter data promptly, resolve queries, and perform corrections to maintain high data quality.
• Coordinate with study teams to receive patient records, lab results, and other source documents.
• Assist in monitoring data accuracy during site visits and audits.
• Support compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.

Required profile

• Bachelor’s degree or equivalent experience in a related field.
• Experience working in a clinical research organization (CRO) or similar environment.
• Strong attention to detail and excellent organizational abilities.
• Effective communication skills for interaction with study teams and monitors.
• Knowledge of clinical trial protocols and regulatory standards.
• CCR or CCRC credentials are highly desirable.

Required skills

• Proficiency in electronic and paper‑based CRF data entry.
• Clinical trial data management.
• Understanding of lab coordination and certification processes (preferred).

What we offer

• Opportunity to contribute to groundbreaking oncology research.
• Professional development within a leading cancer research network.
• Collaborative and inclusive work environment.