Senior Clinical Trial Data Governance Specialist

1 week ago

Sydney, New South Wales, Australia beBeeTransparency Full time $90,000 - $125,000

You will be responsible for overseeing and coordinating redaction activities across multiple teams, requiring a good understanding of clinical trial and submission documents.

Key Responsibilities:
  • Coordinate the operational aspects of transparency activities, including content collection, anonymization, and release.
  • Evaluate data transparency deliverables to ensure they are tracked and published using appropriate systems/tools.
  • Apply relevant data transparency standards, requirements, processes, and policies to comply with health agency regulations.
  • Manage document collections, including indexing and archiving of approved documents.
Requirements:
  • A strong background in the redaction and protection of personal information in the scientific field (pharma, CRO, other).
  • Clinical document specialist/scientific writing support experience is highly desirable.
  • 1-3 years of experience in clinical trial management, regulatory submissions, or publishing would be beneficial.

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