Provide management oversight of drug, biologic, combination product, and consumer product safety activities, and management oversight of applicable pharmacovigilance activities, including adverse event case management, case follow-up; Individual Case Safety Reports (ICSRs), Adverse Drug Reaction (ADR) reporting, periodic safety reporting support and applicable postmarketing safety reporting; MedDRA/IMDRF coding; and safety signal escalation. Manage Medline's adverse event and pharmacovigilance activities for drugs, biologics, combination products, and applicable consumer products, including adverse event case management, assessment, follow-up, documentation, coding, reconciliation, and regulatory reporting.