
11 - 50 employees
⚖️ Legal
🛒 Retail
🤝 B2B
Legal • Retail • B2B
CRS is Civil Recovery Solutions Limited, a company that specializes in civil recovery and civil litigation services. Utilizing a blend of experienced personnel and advanced technology, CRS manages the civil recovery process with high efficiency. The company's tailored solutions are designed to deliver maximized and measurable value, making their service model flexible and easily integrated into various retail environments.
🕒 June 25
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11 - 50 employees
⚖️ Legal
🛒 Retail
🤝 B2B
Legal • Retail • B2B
CRS is Civil Recovery Solutions Limited, a company that specializes in civil recovery and civil litigation services. Utilizing a blend of experienced personnel and advanced technology, CRS manages the civil recovery process with high efficiency. The company's tailored solutions are designed to deliver maximized and measurable value, making their service model flexible and easily integrated into various retail environments.
• 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.
Apply Now🕒 June 24
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🕒 May 26
Junior Clinical Trials Data Specialist at Tempus tasked with reviewing clinical records and managing trial workflows. Collaborating with teams to create accurate, customized clinical reports.