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WorldwideBrasilia, Brazil. Full time.

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PharmacovigilanceClinical trialsAdverse event reportingCompliance and regulatory requirementsStandard operating procedures (SOPs)Data entryRegulatory reportingClinical AssessmentOperational reportingComputer SkillsRelational databaseOrganizational skillsMicrosoft OfficeExcellent verbal and written communicationAttention to detail

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