Ennov CTMS Technical Specialist Wolvio Solutions

About Wolvio Solutions

Job Description

Job Summary: We are seeking a Ennov CTMS Technical Specialist to support, maintain, and enhance our clients enterprise-grade Clinical Trial Management System. This role involves working closely with Clinical Operations, Data Management, IT, and external vendors to ensure that the CTMS and its integrated modules (including Ennov CDM) function reliably, efficiently, and securely across all clinical trial types and organizational needs. Key Responsibilities: System Administration & Configuration Maintain and configure the CTMS platform to support studies from Phase IIV, including decentralized and hybrid trials. Administer system user roles, permissions, and security policies in a 100% web-based environment. Support rapid out-of-the-box implementation and adapt modules to meet project-specific requirements. Implement and test integrations with Ennov Clinical Data Management, mobile monitoring applications, and other clinical systems (e.g., eTMF, EDC). Customize dashboards and alerts to provide clear visibility into investigational site performance and trial progress. Site Monitoring & Mobile Tools Support Provide technical oversight of mobile monitoring apps used by CRAs and field teams. Support real-time data capture enablement by setting up reports, alerting, and dashboarding related to site visit scheduling, trip reports, and issue resolution. Workflow & Task Automation Implement automated task management features to streamline clinical workflows and compliance. Configure alerting systems to support proactive issue resolution and adherence to regulatory timelines. System Monitoring & Reporting Provide visibility into site performance metrics, enrollment status, and operational KPIs via dashboards and reports. Ensure data integrity and audit-readiness of the system. Required Skills and Qualifications: Bachelor's degree in Information Technology, Life Sciences, or a related field. 35 years of hands-on experience with Ennov CTMS. Understanding of clinical trial processes, GCP, and regulatory compliance (e.g., 21 CFR Part 11). Knowledge of Clinical Data Model. Experience with workflow automation tools and system integrations via APIs or middleware. Familiarity with mobile applications used in clinical operations is highly desirable. Excellent problem-solving and communication skills. Ability to work cross-functionally with clinical, data management, and IT teams.,