Tasks

  • Conducting GCP audits in clinical research
  • Creating audit reports and presenting the results
  • Identifying and assessing risks and compliance violations
  • Advising clients on improving their quality management systems
  • Supporting the development and implementation of audit strategies
  • Collaborating with various departments to ensure compliance
  • Conducting follow-up audits to verify the implementation of corrective actions
  • Documenting audit results and creating data analyses to identify trends
  • Actively contributing to the further development of audit methods and processes

Qualifications

  • At least 2-3 years of experience in GCP audits
  • Fluent in English (high level); additional languages such as Italian, French, Spanish, and German are advantageous
  • Knowledge of GCP auditing in clinical studies
  • Team-oriented and communicative personality
  • Ability to work independently and good organizational skills
  • Willingness to travel occasionally within Europe (approximately 2.5 audits per month)