Senior Clinical Business Analyst
21840 - 25200 złLink Group
- Praca zdalna
To stanowisko wymaga obecności na miejscu. Zobacz podobne oferty poniżej.
Key Responsibilities Workshop Facilitation & Discovery: Lead discovery workshops, interviews, and review sessions across Clinical Development business and IT teams. Traceability & Remediation: Reconstruct end-to-end traceability (Requirements Traceability Matrix) linking business intent, functional requirements, system capabilities, and GxP validation evidence. Document & Process Analysis: Evaluate and remediate UERS/URS, FRS, process flows, user stories, and acceptance criteria while resolving gaps, overlaps, or obsolete requirements. Landscape & Dependency Mapping: Map current-state processes and capabilities across Veeva Vault, Medidata, ODR/Snowflake, and adjacent R&D systems. UAT & Validation Alignment: Support UAT preparation (scenario definition, coverage mapping) and collaborate with Validation/CSA SMEs to ensure audit readiness under GxP standards. Governance & Logs: Maintain decision, assumption, risk, and dependency logs while providing BA inputs toward application rationalization. Key Requirements Must-Have: Experience: 7+ years of experience in Business Analysis, Requirements Engineering, or Systems Analysis in senior stakeholder-facing roles. Clinical Domain Expertise: In-depth knowledge of Clinical Development, Clinical Operations, or Clinical Data Management processes and enterprise systems. GxP & Validation: Hands-on experience authoring/remediating UERS/URS, FRS, user stories, and trace matrices in pharmaceutical, life sciences, or GxP-regulated environments. Complex Landscapes: Demonstrated track record working across multi-application, highly integrated enterprise landscapes. Communication: Excellent written and spoken English with top-tier facilitation skills. Nice-to-Have: Hands-on experience with Veeva Vault Clinical applications (multi-vault environments) or Medidata platforms. Understanding of clinical data flows into Snowflake-based data platforms / ODR. Familiarity with GxP validation standards (GAMP 5, 21 CFR Part 11, EU Annex 11, CSA principles). Proficiency with Jira, Confluence, Azure DevOps, or formal requirements repositories.
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