Alterity Therapeutics- Scientific Documentation Specialist

About our Client: Alterity Therapeutics is a dual-listed, late-stage clinical biotechnology company focused on developing disease-modifying treatments for rare and debilitating neurodegenerative disorders About the Role: The Scientific Documentation Specialist provides cross-functional scientific documentation support to help ensure the accuracy, completeness, consistency, traceability, and accessibility of Alterity’s scientific and regulated documentation. The role combines scientific document quality control and source verification with document and information management activities. Based within Regulatory Affairs and Quality Assurance, the role works across Clinical, Nonclinical and Chemistry, Manufacturing and Controls (CMC) to organize and maintain documentation, verify information against designated source materials, and support regulatory submissions, audits, inspections and due diligence. Priorities will be agreed with the line manager in consultation with functional leads. The breadth and focus of responsibilities will evolve based on program priorities, organizational needs, and demonstrated capabilities. Position reports to VP, Regulatory Affairs and Quality Assurance. Key Responsibilities Scientific Documentation and Quality Control Perform documented QC of clinical, nonclinical, CMC and regulatory documents using established procedures and checklists. Verify numerical values, units, tables, figures, references and factual statements against designated source rep