Clinical Research Systems Specialist

Job Summary

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

Key responsibilities

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

Required qualifications

• 3+ years of clinical research experience
• Experience in roles such as CRC, Lead CRC, Research Manager, 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