Clinical Research Systems Specialist

Job Summary

To support the clinical research network, the remote Clinical Research Systems & eSource Specialist will manage the implementation, configuration, and optimization of research systems, providing training and ongoing support to users while ensuring efficient workflows and compliance.

Key responsibilities

• Support daily use and troubleshooting of REALTIME CTMS, eSource, and eRegulatory modules
• Develop and maintain protocol-specific eSource templates and translate study protocols into electronic workflows
• Deliver training on research technology platforms and assist with onboarding new research staff

Required qualifications

• 3+ years of clinical research experience
• Experience as a CRC, Lead CRC, Research Manager, Regulatory Coordinator, or CTMS Administrator
• Familiarity with CTMS, EDC, eSource, eRegulatory, or sponsor systems
• Understanding of clinical trial workflows from feasibility through study close-out
• Experience in training research personnel is preferred