A well seasoned PV professional with a Lead GVP Auditor and EU/EEA Qualified Person for Pharmacovigilance (QPPV) background, having extensive knowledge of all levels of Pharmacovigilance for human and veterinary products, responsible for the overview of medicinal product safety profiles (across multiple therapeutic areas) and any emerging safety concerns, and make decisions in accordance with PV regulations, guidelines and industry best practices.
My current roles involve cross-functional collaboration with multiple departments to meet company set expectations on multiple projects, company business objectives, manage resources, maintain inspection readiness, conduct audits.