Cta-shanghai

IQVIA UK

Shanghai, China
Experience in clinical documentation
Proficient in microsoft office
Knowledge of gcp and ich guidelines
The role involves assisting Clinical Research Associates and Regulatory teams in maintaining clinical documents

Job Summary

  • The role involves assisting Clinical Research Associates and Regulatory teams in maintaining clinical documents.
  • You will help ensure the accuracy of the Trial Master File and manage clinical data flow.
  • IQVIA is committed to integrity in the hiring process and values professionalism.

Matching Summary

The role involves assisting Clinical Research Associates and Regulatory teams in maintaining clinical documents.

Skills & Requirements

Must-have

  • Experience in clinical documentation
  • Proficient in Microsoft Office
  • Knowledge of GCP and ICH guidelines

Nice-to-have

  • Effective communication skills
  • Strong organizational abilities
  • Ability to work in a team

Key Requirements

  • High School Diploma or equivalent
  • 3 years administrative support experience
  • Good command of English language

Work Rights

Not specified

Tailored Resume

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