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SareptaCambridge, MA, United States. Full time.

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PharmacovigilanceRisk managementClinical DevelopmentClinical trialsMonitoringUtilization ReviewAdverse event reportingStatistical analysis plan developmentClinical study report authoringRegulatory submissionsClinical experienceExcellent verbal and written communicationDecision-makingMultitaskingAttention to detail

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