
11 - 50 employees
Civil Recovery Solutions Limited (CRS) offer the next generation in specialist civil recovery and civil litigation services. CRS combines a team of highly experienced personnel with powerful new technology and bespoke tools to manage the civil recovery process extremely effectively and efficiently. The easily integrated CRS model is radically different and flexible; it provides a tailored solution ensuring maximised and measurable value from a civil recovery strategy.
🔥 1 minute ago
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11 - 50 employees
Civil Recovery Solutions Limited (CRS) offer the next generation in specialist civil recovery and civil litigation services. CRS combines a team of highly experienced personnel with powerful new technology and bespoke tools to manage the civil recovery process extremely effectively and efficiently. The easily integrated CRS model is radically different and flexible; it provides a tailored solution ensuring maximised and measurable value from a civil recovery strategy.
• Identify, document, and triage system issues or user‑reported bugs in the in‑house EDC platform. • Support the implementation and verification of fixes and enhancements with Software Development. • Perform initial root‑cause analysis for Azure‑based issues before escalating. • Translate Data Management needs into actionable tickets, requirements, or feature requests. • Support form testing, CRF logic verification, and data query workflows. • Create and execute test scripts as part of system validation and release cycles. • Maintain accurate system documentation, user guides, and training resources. • Participate in regular Software–DM syncs to stay aligned on priorities and release plans. • Deliver user training and frontline support for clinical study teams.
• Bachelor’s degree in Life Sciences, Computer Science, Health Informatics, or related field. • 1–3 years in clinical data management, clinical systems support, clinical research technology, or software QA within a clinical research environment. • Exposure to EDC platforms (REDCap, Medidata, OpenClinica, or homegrown). • Familiarity with Microsoft Azure tools (Azure SQL, Azure DevOps, Functions • Understanding of FDA 21 CFR Part 11, ICH‑GCP, and clinical data documentation standards. • Basic understanding of relational databases and structured data (SQL a plus). • Strong communication, documentation discipline, and cross‑team collaboration abilities. • High attention to detail and strong organization in a fast‑moving environment. • Ability to perform User Acceptance Testing (UAT) to ensure new features and fixes meet intended requirements.
• Occasional domestic travel may be required for company meetings, audits, etc.
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