飩稯ver 5 years of experience working in Pharmaceutical, Clinical Research & Pharmacovigilance industry with hands-on experience in Oracle Clinical Data Management & Oracle Argus Adverse Event Reporting System.
飩稥xtensive experience in SAE Case processing which includes聽Case Validation, Case Data Entry from spontaneous, literature, and clinical trial cases within safety system, Quality Check, Safety Narrative Writing, and Medical Coding.
飩稰roficient in Medical Assessment i.e. Seriousness, Signal Detection, Completeness, Accuracy and Appropriateness of safety reports.
飩稥xcellent knowledge of different levels of Medical coding for adverse events as per MedDRA and WHODRUG dictionaries.
飩稥xcel...
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