An enthusiastic and high energy driven professional seeking positions and challenging assignments in Pharmacovigilence & drug safety, life sciences, clinical reserach, medical writing and data analytics.
Knowledge of global Pharmacovigilence database ARISg, processing of individual Case Safety Reports (ICSRs) originating from various sources, post-marketing non-solicited reports/Spontaneous reports, Clinical trial reports, E2B reports.
Triage and tracking all cases, Initial and final regulatory assessments, MedDRA and WHO-drug coding, case narrative. Development and maintenance of Analysis of Similar Events, Complete medical monitoring and follow-up support, processing of expedited IC...
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