CRIO eSource Designer

CRIO eSource Designer Monroe+Biomedical+Research Charlotte, NC Job Details Full-time 14 hours ago Qualifications Clinical research Data collection Full Job Description CRIO eSource Specialist/Coordinator Position Summary Monroe Biomedical Research is seeking a detail-oriented and experienced

REMOTE CRIO

eSource Specialist to support the development and maintenance of electronic source documentation for clinical trials across a growing research network. This role is responsible for translating clinical study protocols, sponsor requirements, and visit schedules into organized, user-friendly source templates that support accurate and efficient data collection at the site level. The ideal candidate has hands-on experience building within the CRIO platform, understands clinical research operations, and thrives in a fast-paced, collaborative environment. Key Responsibilities eSource Development & Study Build Design and configure electronic source templates within CRIO based on study protocols and sponsor requirements Review schedules of assessments, annotated CRFs, EDC guidelines, and sponsor materials to identify required study data points Create visit-specific source workflows that align with coordinator processes and study timelines Ensure source builds support accurate data capture while minimizing duplicate entry and workflow inefficiencies Study Documentation & Quality Maintain standardized formatting and documentation practices across studies and research sites when appropriate Conduct quality reviews of source builds prior to site activation and study launch Revise and maintain source documentation following protocol amendments, sponsor updates, or operational changes Ensure documentation supports regulatory compliance and Good Clinical Practice (GCP) expectations Cross-Functional Collaboration Partner with Clinical Research Coordinators, Site Managers, Regulatory staff, and Operations leadership to support study implementation Provide timely delivery of completed source builds for site review and activation timelines Assist with troubleshooting workflow or documentation-related issues within CRIO as needed. Qualifications Required Prior experience building electronic source documentation within CRIO Clinical research experience in a role such as Clinical Research Coordinator, Data Manager, Regulatory Specialist, or similar Strong understanding of clinical trial workflows, protocol structure, and study visit schedules Familiarity with sponsor EDC systems and clinical trial documentation requirements Strong organizational skills and exceptional attention to detail Ability to work independently in a remote environment while managing multiple priorities Preferred Experience supporting multiple clinical research sites or study teams Familiarity with annotated CRFs and sponsor completion guidelines Knowledge of GCP standards and source documentation best practices Experience supporting study start-up or activation processes Key Skills CRIO eSource configuration and workflow design Clinical protocol interpretation Study documentation management Process organization and workflow optimization Cross-functional communication and collaboration Quality review and version control Position Details Full-time with comprehensive benefits package Remote position Reports to: SVP of Operations This position is open only to candidates legally authorized to work and currently residing in the United States. Additional Information Candidates will be required to answer CRIO-specific screening questions as part of the interview process.