Clinical QA Auditor: GCP/GMP Compliance

Iovance Biotherapeutics in Dubai seeks a Clinical Quality Assurance professional to support audits of investigational sites, internal systems and trial master files, ensuring GCP compliance.

You will plan, coordinate, and report audits, escalate critical observations, and collaborate across functions to drive inspection readiness and process improvements. This role requires 1+ year GCP/GMP experience and familiarity with MasterControl or Veeva; UAE work authorization preferred.