Remote Document Specialist (Veeva Vault & QC)

Confedential

South Africa

A distancia

ZAR 300.000 - 420.000

Jornada completa

Hace 5 días
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Ventajas ofrecidas por este puesto de trabajo

Laptop provided
Remote work aligned with US time zones
Introductory training and onboarding

Descripción de la vacante

Peritia is seeking a Document Specialist Consultant to support the Medical Writing team in management and quality control of clinical and regulatory documents. The role focuses on eDMS workflows, templates, and metadata in a fast-paced biopharma setting.

The ideal candidate will have hands-on Veeva Vault experience, strong Word/Excel skills, and the ability to collaborate across departments while ensuring inspection readiness and compliance.

Formación

  • 3+ years of technical documentation experience in pharma/biotech or 1.5+ years with an advanced degree
  • Strong understanding of clinical development and regulatory documentation
  • Hands-on experience with eDMS platforms (Veeva Vault or similar)
  • Advanced Word skills: complex formatting, styles, templates

Responsabilidades

  • Manage creation, routing, review, approval, versioning and archiving of clinical/regulatory documents
  • Ensure adherence to templates, naming conventions, metadata and folder structures
  • Perform eQC reviews for CSRs, protocols, integrated summaries, HA responses
  • Maintain document records and support traceability
  • Collaborate with Medical Writing, Regulatory Affairs and Clinical Operations
  • Support audit/inspection readiness and compliance

Conocimientos

Document management
Quality control
eDMS
Veeva Vault
MS Word
MS Excel
Adobe Acrobat
Communication
Cross-functional collaboration

Educación

Bachelor’s degree
Advanced degree (preferred)

Herramientas

Veeva Vault

Descripción del empleo

Peritia is seeking a Document Specialist Consultant to support the Medical Writing team in management and quality control of clinical and regulatory documents. The role focuses on eDMS workflows, templates, and metadata in a fast-paced biopharma setting.

The ideal candidate will have hands-on Veeva Vault experience, strong Word/Excel skills, and the ability to collaborate across departments while ensuring inspection readiness and compliance.

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