Document Anonymization Specialist

GSK

Not specified
Master's degree in life sciences or related field
6-9 years experience in document anonymization
Knowledge of ema policy 0070 and health canada prci
GSK is seeking a Document Anonymization Specialist to lead activities that support ethical sharing of clinical research data. The role requires expertise in document anonymization and a strong understanding of regulatory requirements, with opportunities for career development and impacting public trust in research

Job Summary

  • This role leads document anonymization activities to support ethical and transparent sharing of clinical research data while aligning with GSK's mission to positively impact the health of 2.5 billion people.
  • The specialist serves as a subject matter expert on regulatory requirements, managing daily operations to ensure quality and timeline targets are met for both current and historical studies.
  • Candidates will build strong working relationships with internal teams and external vendors, fostering a culture of quality, transparency, and continuous improvement in clinical data re-use.

Matching Summary

Match Score: 85

GSK is seeking a Document Anonymization Specialist to lead activities that support ethical sharing of clinical research data. The role requires expertise in document anonymization and a strong understanding of regulatory requirements, with opportunities for career development and impacting public trust in research.

Skills & Requirements

Must-have

  • Master's degree in life sciences or related field
  • 6-9 years experience in document anonymization
  • Knowledge of EMA Policy 0070 and Health Canada PRCI
  • Experience managing clinical trial activities
  • Understanding of clinical trial lifecycle and metadata

Nice-to-have

  • Ability to bridge scientific and non-scientific communication gaps
  • Proactive process improvement mindset
  • Strong influence skills across global functions
  • 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 of experience in document anonymization or clinical trial transparency
  • Experience in pharmaceutical company matrix organization
  • Expertise in regulatory policies like EMA Policy 0070

Work Rights

Not specified

Tailored Resume

Cover Letter