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Link Group

Senior Clinical Business Analyst

Szczecin
Białystok
Warszawa
Poznań
+7
Läuft ab 29 Nov 2026
vor 6 Tagen

Kurzfassung

Senior Clinical Business Analyst sought for Link Group in Szczecin. Responsibilities include workshop facilitation, requirements engineering, and process analysis within Clinical Development. Requires 7+ years BA experience, GxP knowledge, and clinical domain expertise.

Von KI erstellte Kurzfassung des Anzeigentextes.

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.
Veröffentlicht 2026-10-28
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