Clinical Systems Designer (PST/EST/CST Timezone)

Job Description: Clinical Systems Designer 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.

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.

- 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.

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.