Clinical Trials Disclosure Specialist

3 days ago


Lawrence, Kansas, United States Net2Source Inc. Full time
Job Title: Clinical Trials Disclosure Specialist

Net2Source Inc. is a leading provider of total workforce solutions, recognized for our accelerated growth and commitment to addressing the current talent gap. We believe in providing staffing solutions that meet the needs of our clients and candidates.

Job Summary:

The Clinical Trials Disclosure Specialist will provide operational support for the redaction of clinical trial documents in accordance with evolving global regulations. This role will collaborate with internal stakeholders to operationalize redaction requirements and provide vendor oversight to support document redactions.

Key Responsibilities:

  • Manage and coordinate redaction of clinical documents in accordance with EMA Policy 0070, Health Canada Public Release of Clinical Information (PRCI), EU Clinical Trial Regulation, and other global regulations.
  • Collaborate with Global Development Operations, Global Biostatisticians, Medical Writing, Submission Managers, and other stakeholders to operationalize redaction requirements.
  • Provide vendor oversight to support document redactions.
  • Work with IT, as needed, to implement technology solutions related to clinical trial disclosure.
  • Manage and track redaction book-of-work; compile and report on volume and performance metrics.
  • Provide operational support to CT Results Specialists, as required.
  • Assists in monitoring the global regulatory environment and maintains working knowledge of disclosure requirements.
  • Communicates with internal and external stakeholders to improve on processes and manage unmet need.
  • Trains new staff and develops job aids, work instructions, and user guides, as needed.

Candidate Requirements:

  • BA/BS or MA/MS in scientific or medical field.
  • 2-3 years of document redaction and 3+ years relevant work experience in a scientific or medical field with BA/BS.
  • Deep understanding of US/Canada and EU requirements for clinical trial disclosure as well as other related policies (ICMJE, PhRMA/EFPIA principles for responsible data sharing, etc.).
  • Familiarity and comfortability working with and discussing scientific data.
  • Project and stakeholder management experience.
  • Demonstrated ability to work independently and seek out support when needed.
  • Exceptional written and oral communication skills.
  • Strong organizational skills with the ability to multitask and prioritize.


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