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I have clinical experience in reporting post-marketing events in the pharmaceutical industry, comprehensive knowledge of Health Canada and ICH safety reporting regulations(ICH-GCP- DIVISION 5 and CFR) and international drug safety and pharmacovigilance principles. • Remarkable knowledge to monitor and track Serious Adverse Events, serious and non-serious adverse drug reactions, and other medically related project information Highly motivated with burning desire to work in clinical research industry specifically pharmacovigilance sector but not limited to. Recently, in Aug 2015 certified with TCPS2:CORE (online course on Research ethics). ...