Senior Clinical Trial Transparency Expert

1 week ago

Sydney, New South Wales, Australia beBeeClinical Full time $140,000 - $180,000

Job Overview

This role plays a pivotal part in ensuring transparency across clinical trials. The successful candidate will oversee and coordinate redaction activities, collaborating with various teams to achieve this goal.

Main Responsibilities

  • Coordinate the operational aspects of transparency activities, including content collection for redaction/anonymization and partnerships with anonymization providers.
  • Ensure timely publication of data transparency deliverables using appropriate systems/tools.
  • Apply relevant standards, requirements, processes, and policies to comply with health agency regulations.
  • Provide document management services, including indexing and archiving approved documents.

Requirements

  • Experience in protecting personal information in scientific contexts (pharma, CRO, etc.) is required.
  • Clinical document specialist/scientific writing support experience is highly valued.
  • 1-3 years of experience in clinical trial management, regulatory submissions, or publishing are preferred.
  • Basic understanding of clinical trial or submission document disclosure requirements.
  • Knowledge of electronic document management systems and proficiency in Adobe Acrobat.
  • Proficiency in disclosure-related Health Authority and industry regulations and guidelines.

What We Offer

  • A competitive salary and additional benefits focused on well-being and work-life balance.
  • Annual leave entitlements, health insurance offerings, retirement planning, and more.

About Our Culture

  • We maintain an inclusive and accessible environment for all candidates.
  • We are committed to providing a workplace free from discrimination and harassment.

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