Auditor (Contract) Position

4 days ago

London, Greater London, United Kingdom ProPharma Group Full time
Job Title: GVP Auditor

ProPharma Group is seeking a highly skilled GVP Auditor to join our team. As a subject matter lead for clinical consulting and auditing projects, you will be responsible for executing audits based on your experience and comprehensive understanding of federal regulatory requirements and ICH guidance on Good Clinical Practice (GCP) and Good Pharmacovigilance Practices (GVP).

Key Responsibilities:
  • Conduct audits and provide oversight/management of the GVP consulting program.
  • Keep pace with advances and technological changes in clinical support services within the pharmaceutical/device/biotech industries and promote those that will increase the company's effectiveness and profits.
  • Provide support to clients and all functional units of ProPharma Group as clinical compliance issues such as deviations and non-conformances arise.
  • Ensure compliance of company operations to quality principles and participate in the development of quality systems through SOP writing and training.
  • Promote GVP subject expertise through publications and presentations through professional networks.
  • Provide ongoing support and expertise to all personnel, assisting them in establishing goals, objectives, policies, and procedures for all applicable subsets of this business unit within the company.
  • Ensure consulting practices are in compliance with all applicable internal and external policies procedures, and industry best practices.
  • Generate proposals for GVP auditing and clinical-related projects.
  • Audit GVP projects for correct approach, consistency, and quality.
  • Organize and manage projects with quality orientation and high attention to detail.
Requirements:
  • University degree in scientific discipline as a minimum.
  • Minimum 10 years of clinical compliance and GVP auditing experience in related industry.
  • Minimum 5 years managing a technology business or business unit or applicable related experience.

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