Core ICF Developer/Writer and Reviewer - São Paulo

Apenas para membros registrados São Paulo, Brasil

há 1 semana

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Job summary

Developing reviewing finalizing and maintaining clinical trial documents such as informed consent forms. Ensures client-specific guidance and requirements are included within the Master Informed consent form during development and review.

Responsible for timely appropriate communication to all stakeholders as applicable Liaise with PM/Designee to communicate any trends outstanding issues safety concerns or any other activity or lack thereof that may jeopardize the clinical trial delivery or patient safety from the task assigned.


Create review revise training material plans to support the training requirements of the team.


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