Clinical Systems Designer (PST/EST/CST Timezone)
On-siteCairo, Cairo, Egypt
Job Summary
Translate study protocols into compliant e-source templates and build visit schedules, assessments, and workflows in CRIO, Clinical Conductor, and RealTime CTMS. Develop and maintain electronic regulatory binders while mapping procedures to financial tracking for accurate billing and site invoicing. Perform quality control checks, gather feedback from coordinators and investigators, and update builds to ensure adherence to FDA, ICH-GCP, and 21 CFR Part 11 regulations. Establish SOPs and best practices for e-source processes, provide training on CTMS builds, and maintain full version control for all study documentation.
Required Qualifications
- Bachelor's degree in Life Sciences, Clinical Research, or related field (or equivalent experience)
- At least 1 year of direct experience building e-source and e-regulatory in CRIO (required)
- Strong understanding of clinical trial protocols, regulatory compliance, and site operations
- Ability to map procedures to budgets/financials in CTMS platforms
- Strong attention to detail, documentation, and version control
- Excellent communication and collaboration skills
Desired Qualifications
- Experience performing e-source and e-regulatory builds in Clinical Conductor and/or RealTime CTMS (strongly preferred)
- Experience across multiple CTMS/EDC platforms (with e-source build responsibilities)
- Process optimization and SOP development experience
- Knowledge of site-level finance, billing, and reconciliation workflows
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