Clinical Trial Support Specialist

Há 4 dias


Oeiras, Lisboa, Portugal IQVIA Argentina Tempo inteiro
About the Role

This Study Management Assistant position is responsible for assisting Clinical Research Associates (CRAs) and Regulatory and Start-Up team members with accurately updating and maintaining clinical documents and systems like Trial Master File that track site compliance and performance within project timelines. Key responsibilities include assisting with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.


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