Position Summary

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.