Regulatory requirements for document anonymization
You will lead document anonymisation activities that support ethical and transparent sharing of clinical research data
Job Summary
You will lead document anonymisation activities that support ethical and transparent sharing of clinical research data.
Manage daily operations of anonymizing clinical documents including regulatory requirements like EMA Policy 0070 and Health Canada PRCI ensuring quality and timelines targets are met.
This role offers clear career development, meaningful impact on public trust in research, and alignment with GSK’s mission of uniting science, technology and talent to get ahead of disease together.
Matching Summary
You will lead document anonymisation activities that support ethical and transparent sharing of clinical research data.
Skills & Requirements
Must-have
document anonymisation activities
clinical research data sharing
regulatory requirements for document anonymization
EMA Policy 0070 and Health Canada PRCI
process improvements based on feedback
Nice-to-have
growth mindset
public trust in research
uniting science technology talent
industry and regulatory standards
Key Requirements
Master’s degree in life sciences, pharmacy, clinical research, or a related field