Transparency Specialist - Document Anonymization

GSK

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Clinical trial transparency
Document anonymisation
Regulatory requirements
** GSK is seeking a Transparency Specialist to lead document anonymization activities that ensure ethical sharing of clinical research data. The role entails collaboration with cross-functional teams and external partners, focusing on compliance with regulatory requirements while fostering a culture of quality and transparency. **

Job Summary

  • You will lead document anonymisation activities that support ethical and transparent sharing of clinical research data.
  • 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.
  • You deliver anonymised documents consistently and on time.

Matching Summary

Match Score: 75

** GSK is seeking a Transparency Specialist to lead document anonymization activities that ensure ethical sharing of clinical research data. The role entails collaboration with cross-functional teams and external partners, focusing on compliance with regulatory requirements while fostering a culture of quality and transparency. **

Skills & Requirements

Must-have

  • clinical trial transparency
  • document anonymisation
  • regulatory requirements
  • vendor management
  • cross-functional collaboration

Nice-to-have

  • growth mindset
  • ambitious for patients
  • technical care
  • public trust in research
  • community of practice

Key Requirements

  • Master’s degree in life sciences, pharmacy, clinical research, or related field
  • 6 - 9 years' experience in document anonymisation
  • Experience in Pharmaceutical company environment
  • Experience managing clinical trial activities
  • Good understanding of clinical trial lifecycle and data

Work Rights

Not specified

Tailored Resume

Cover Letter