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Iqvia seeks a Pharmacovigilance Regulatory Reporting specialist to process safety data for regulatory submissions and ensure SOP and project compliance. You will coordinate reporting to regulatory authorities and internal partners while working with cross-functional teams.
This remote, multilingual role supports pharmacovigilance activities in English, Spanish, and Portuguese, offering meaningful impact on patient safety within a global network and opportunities to collaborate with healthcare
Iqvia seeks a Pharmacovigilance Regulatory Reporting specialist to process safety data for regulatory submissions and ensure SOP and project compliance. You will coordinate reporting to regulatory authorities and internal partners while working with cross-functional teams.
This remote, multilingual role supports pharmacovigilance activities in English, Spanish, and Portuguese, offering meaningful impact on patient safety within a global network and opportunities to collaborate with healthcare