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WorldwideBuenos Aires, Argentina; Brasilia, Brazil. Full time.

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Clinical trialsRegulatory submissionsMedical History TakingGCPRequirements AnalysisRegulatory affairsRAMRegulatory requirementsRegulatory change monitoringCopy editingExcellent verbal and written communicationInterpersonal SkillsMicrosoft WordClinical researchWorking unsupervised

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