Safety & PV Submission Spec I

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Safety & PV Submission Spec I based in Brazil. In this role, you will support the preparation, coordination, and submission of critical pharmacovigilance and drug safety reports to regulatory authorities, ethics committees, and clinical investigators. You will contribute to ensuring that safety documentation is accurate, complete, and submitted within established r…

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