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  • ID
    #51421014
  • Job type
    Full-time
  • Salary
    TBD
  • Source
    AbbVie
  • Date
    2024-03-28
  • Deadline
    2024-05-27
 
Full-time

providing clinical regulatory document support and advanced scientific writing expertise to the clinical teams, ensuring successful AMWA) certification or other is preferred, with a specialty in Editing/Writing or Pharmaceutical.

4 years relevant industry experience

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