Quality Management Associate - Europe - Remote

Worldwide Clinical Trials

Multiple Locations
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Quality management system (qms)
Quality issues (qis)
Corrective and preventive action (capa)
** The Quality Management Associate position at Worldwide Clinical Trials is a remote role aimed at individuals with a background in quality assurance within the clinical research industry. The ideal candidate will have experience in Good Clinical Practice (GCP), strong communication skills, and a proactive approach to quality management. **

Job Summary

  • Champions the adoption of the Quality Management System (QMS).
  • Provides consultancy and oversight for project-specific Quality Issues (QIs) and Corrective and Preventive Action (CAPA) Plans.
  • Acts as GCP/GLP/GcLP Subject Matter Expert (SME), provides GCP/GLP/GcLP consultancy to project teams.

Matching Summary

Match Score: 75

** The Quality Management Associate position at Worldwide Clinical Trials is a remote role aimed at individuals with a background in quality assurance within the clinical research industry. The ideal candidate will have experience in Good Clinical Practice (GCP), strong communication skills, and a proactive approach to quality management. **

Skills & Requirements

Must-have

  • Quality Management System (QMS)
  • Quality Issues (QIs)
  • Corrective and Preventive Action (CAPA)
  • GCP/GLP/GcLP consultancy
  • ICH Guidelines
  • FDA Code of Federal regulations
  • European Directives
  • UK Statutory Instruments

Nice-to-have

  • positive QA ambassador
  • sense of urgency
  • flexible approach
  • Risk Based Quality Management

Key Requirements

  • College/University degree or equivalent
  • 2+ years of relevant GCP experience
  • IT literate, proficient in Excel, Word, SharePoint, PowerPoint
  • Domestic and international travel may be required (not exceeding 10%)

Work Rights

Not specified

Tailored Resume

Cover Letter