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Primary Areas of Responsibility: Create and revise documentation related to clinical trials including protocols, user manuals, reference guides, newsletters, etc Create and revise documentation related to procedures including SOPs, work instructions, etc Create training materials for external collaborators in healthcare centers globally Gathering user requirements for software applications and writing Functional Requirement Specifications (FRS) documentsContinue Reading > Read Full Description
Confirmed 16 days ago. Posted 30+ days ago.

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