Job Description

We are supporting a leading CRO / consultancy in their search for an experienced QA-IT / Computer System Validation (CSV) Consultant to support GxP and GCP-regulated systems within a clinical environment.

This is a contract role suited to someone confident operating independently and partnering closely with Process and System Owners to ensure compliance, data integrity, and high-quality validation outcomes.

Key Responsibilities

  • Support the Process and System Owner in the planning and execution of CSV activities in line with GxP / GCP requirements
  • Create, review, and maintain full validation documentation , including:
  • Validation Plans
  • User Requirements Specifications (URS)
  • Validation Reports
  • Ensure traceability, consistency, and audit readiness across all validation documentation
  • Support compliance with data integrity principles throughout system lifecyc...

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