Job Details

Zusammenfassung

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Job Details

Ihre Aufgaben

  • Independently leading all activities from assessment, planning, and conceptual realization to implementation, review, maintenance, and decommissioning of study-specific IRT concepts
  • Acting independently as an IRT representative in cross-organizational and cross-functional study and project teams
  • Ensuring that all technical implementations of IRT concepts are performed in compliance with drug safety, GMP, GCP, as well as US, EU, and other international guidelines
  • Contributing to the continuous development of IRT concepts by bringing in new approaches and solutions to keep systems state-of-the-art
  • Supporting computerized system validation (CSV) activities

Ihr Kontakt

Kontaktieren Sie uns wenn Sie weitere Fragen haben.

RK

Robert Kimont

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