Document Anonymization Specialist

GSK

Not specified
6-9 years experience in document anonymisation
Master's degree in life sciences or related field
Knowledge of ema policy 0070 and health canada prci
GSK is seeking a Document Anonymization Specialist to lead the ethical sharing of clinical research data while ensuring compliance with regulatory requirements. The role emphasizes collaboration, technical expertise, and a commitment to improving processes to enhance public trust in research

Job Summary

  • This role leads document anonymization activities that support ethical and transparent sharing of clinical research data within GSK's R&D division.
  • The successful candidate will serve as a subject matter expert on regulatory requirements including EMA Policy 0070 and Health Canada PRCI.
  • You will manage daily operations of anonymizing clinical documents while maintaining strong relationships with internal business partners and external vendors.

Matching Summary

Match Score: 85

GSK is seeking a Document Anonymization Specialist to lead the ethical sharing of clinical research data while ensuring compliance with regulatory requirements. The role emphasizes collaboration, technical expertise, and a commitment to improving processes to enhance public trust in research.

Skills & Requirements

Must-have

  • 6-9 years experience in document anonymisation
  • Master's degree in life sciences or related field
  • Knowledge of EMA Policy 0070 and Health Canada PRCI

Nice-to-have

  • Ability to bridge scientific and non-scientific communication gaps
  • Experience reviewing clinical documents
  • Awareness of medical writing and publishing processes

Key Requirements

  • Master's degree in life sciences, pharmacy, or clinical research
  • 6-9 years experience in document anonymisation or clinical trial transparency
  • Experience in pharmaceutical company environment and matrix organization

Work Rights

Not specified

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