Clinical Research Systems – eSource Specialist

This is a fully remote position, open to applicants in United States.

📋 Description

• Provide daily support for the use of REALTIME CTMS, eSource, and eRegulatory modules.

• Assist users with system navigation, troubleshooting, and inquiries regarding workflows.

• Aid in the implementation of new research technologies and sponsor systems.

• Engage in system testing, validation, and activities aimed at optimizing workflows.

• Help manage user accounts and process access requests.

• Develop and maintain eSource templates specific to protocols.

• Convert study protocols into effective electronic workflows.

• Create visit-specific source documentation.

• Configure forms, templates, workflows, and tools for data collection.

• Standardize eSource practices across various research sites.

• Assess coordinator workflows and pinpoint areas for enhancement.

• Provide training on REALTIME and research technology platforms.

• Create user guides, job aids, and training materials.

⛳️ Requirements

• Minimum of 3 years of experience in clinical research.

• Background as a CRC, Lead CRC, Research Manager, Regulatory Coordinator, or CTMS Administrator.

• Familiarity with CTMS, EDC, eSource, eRegulatory, or sponsor systems.

• Experience in creating source documents and visit worksheets.

• Understanding of clinical trial workflows from feasibility through to study close-out.

• Experience in training research personnel is preferred.

🏝️ Benefits

• Competitive salary.

• Health insurance.

• Flexible working hours.

• Opportunities for professional development.

• Training on system administration.

• Ongoing coaching and support.