Safety Physician with three years PV experience in providing medical review and assessment of individual case safety reports from clinical trials, post-marketing, and literature review for seriousness, expectedness and causality. * Strong knowledge of pharmacovigilance, including safety regulations (US and EU guidelines, E2A, E2BM, Vol 9A) and drug safety assessment (triage and MedDRA coding, WHO DD, data mining, as well as aggregated safety signal detection and assessment). Strength in identifying and evaluating safety signals based on individual cases and cumulative data assessment, risk management plans (RMP) and safety aggregate reporting (DSUR and PSUR). * More than ten years of medical training and clinical practice in Internal Medicine with specialization in Cardiology in China. * Recognized for ability to work collaboratively across teams. Served as a strategic leader. * Effective verbal and written communication skills along with extensive scientific publications (See below).