Conduct the assessment of all serious individual adverse event case reports stemming from pre-clinical studies, post-marketed and literature sources. Performs quality control of key data fields, and makes updates in the safety database per process conventions Executes case assessment (review events, determine expectedness, review/update drug and medical term coding, determine causality) Creates clear, medically concise case narrative procured from relevant information in form of various source documents Drafts pharmacovigilance company comment Determines follow-up actions and generates letters/queries as appropriate
https://www.indeed.com/viewjob?t=drug+safety+specialist&jk=e0a8f642e0d79a81&_ga=2.45614436.1326352972.1562606511-1429968906.1557248850
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