Remote Scientific Documentation Specialist for Regulatory QA

Alterity Therapeutics Limited

United States

Remote

USD 70,000 - 110,000

Full time

7 days ago
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Job summary

Alterity Therapeutics is seeking a remote US-based Document Control Specialist to support Regulatory Affairs and QA teams in clinical, nonclinical, and CMC areas. You will QC scientific documents, manage repositories, and prepare submission packages for audits and inspections.

The role requires a life sciences degree and experience with regulated documentation, along with strong attention to detail and MS Office proficiency.

Qualifications

  • Bachelor's degree in life sciences, biomedical sciences, chemistry, pharmacology, or related discipline.
  • Experience with scientific document QC, regulated documentation, or document management is preferred.
  • Strong attention to detail, analytical ability, and proficiency with Microsoft Word, Excel, and PowerPoint.

Responsibilities

  • Provide cross-functional scientific documentation support to ensure accuracy, completeness, and traceability.
  • Work within Regulatory Affairs and Quality Assurance to support clinical, nonclinical, and CMC teams.
  • Perform QC checks on scientific and regulated documents using established procedures and checklists.
  • Manage document repositories, filing structures, metadata, and workflows in systems like SharePoint and Veeva.
  • Prepare and retrieve document packages for regulatory submissions, audits, inspections, and due diligence.

Skills

Scientific document QC
Regulated documentation
Document management

Education

Bachelor's degree in life sciences or related discipline

Tools

MS Word
MS Excel
PowerPoint

Job description

Alterity Therapeutics is seeking a remote US-based Document Control Specialist to support Regulatory Affairs and QA teams in clinical, nonclinical, and CMC areas. You will QC scientific documents, manage repositories, and prepare submission packages for audits and inspections.

The role requires a life sciences degree and experience with regulated documentation, along with strong attention to detail and MS Office proficiency.

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