[Hiring] Clinical Systems Designer @Indeed

Role Description

We are seeking a detail-oriented E-Source Builder with hands-on experience designing and maintaining electronic source documents and e-regulatory binders in CRIO (required). The ideal candidate will also have experience performing the same role in Clinical Conductor and/or RealTime CTMS, including study build-out, procedure mapping, financial integration, and regulatory binder setup. This role is essential to ensuring studies are configured accurately and efficiently across systems, supporting both compliance and operational excellence.

Key Responsibilities

• Study Build-Out
  • Translate study protocols into compliant, user-friendly e-source templates in CRIO.
  • Build study visit schedules, assessments, procedures, and workflows in CRIO, and ideally in Clinical Conductor and RealTime as well.
  • Ensure builds meet sponsor/CRO requirements and site operational needs.
• E-Regulatory Setup & Compliance
  • Develop and maintain electronic regulatory binders in CRIO, with preference for experience doing the same in Clinical Conductor and RealTime.
  • Ensure compliance with FDA, ICH-GCP, and 21 CFR Part 11 regulations.
  • Standardize filing procedures and QC document uploads.
• Financials & Budget Integration
  • Map study procedures to financial tracking in CRIO, with the ability to replicate this process in Clinical Conductor and RealTime.
  • Collaborate with finance teams to align billing with study requirements.
  • Ensure contracted budgets are accurately linked to procedures and site invoicing.
• Quality & Process Improvement
  • Develop SOPs and best practices for e-source and e-regulatory build processes.
  • Perform QC checks, gather coordinator/investigator feedback, and update builds accordingly.
  • Maintain full documentation and version control for study builds.
• Collaboration & Training
  • Partner with Clinical, Regulatory, and Finance teams to deliver accurate builds.
  • Provide training, support, and troubleshooting for CRIO and other CTMS builds.

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).
• Experience performing e-source and e-regulatory builds in Clinical Conductor and/or RealTime CTMS (strongly preferred).
• 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.

Preferred Skills

• 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.

Key Success Metrics

• Accuracy and compliance of e-source and e-regulatory builds.
• Timely completion of study build-outs.
• Reduction in errors, deviations, or billing mismatches.
• Positive feedback from coordinators, investigators, and regulatory staff.