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Zusammenfassung

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Job Details

Ihre Aufgaben

  • Define early disclosure strategies at study concept and protocol stages as well as during amendment stages
  • Prepare, review, and submit clinical trial registrations across global registries such as CTIS and ClinicalTrials.gov
  • Maintain accurate, up-to-date, and compliant registry records throughout the entire study lifecycle
  • Coordinate the creation and submission of clinical trial results disclosures
  • Ensure full inspection readiness through precise documentation and auditable evidence
  • Support data quality, system maintenance, and vendor oversight activities

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