Sana Hameed

At AbbVie, I support pharmacovigilance reporting, follow-up workflows, quality control dashboards, Argus Live access, and documentation that supports regulatory submissions. I coordinate with cross-functional and IT teams to resolve data issues, improve quality-control functionality, and maintain accurate adverse event information.

Previously at Genentech, I performed CAPA audits, literature surveillance, SAE reconciliation, adverse-event quality checks, and AESI trend analysis. I also supported audit readiness, team training, safety-signal assessment, and drug safety initiatives aligned with regulatory and operational requirements.