Trial Master File Specialist

hace 7 días


Buenos Aires, Buenos Aires C.F., Argentina Iqvia A tiempo completo
Key Responsibilities
A Clinical Trial Assistant will be responsible for providing administrative support to the Clinical Research Associates and Regulatory and Start-Up teams. Key responsibilities include:
  • Updating and maintaining clinical documents and systems.
  • Preparing, handling, distributing, filing, and archiving clinical documentation and reports.
  • Maintaining site compliance and performance within project timelines.
The ideal candidate will have a life science degree, clinical research experience, and excellent communication skills.

Requirements

  • Life science degree or equivalent combination of education and experience.
  • Clinical research experience is highly valued.
  • Excellent computer skills including Microsoft Word, Excel, and PowerPoint.
  • Effective time management and organizational skills.
  • Awareness of applicable clinical research regulatory requirements.


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