Applicant must have Masters degree or U.S. equivalent in Pharmacology or Pharmacy. Applicant must have 2 years of work experience in Clinical Safety within the pharmaceutical industry. Applicant must have experience in clinical safety case Processing by using safety databases and Clinical databases such as INFORM, Oracle RDC, and Enable; coding with MedDRA and drugs with WHO drug dictionaries; and performing reconciliation of case safety events. Must have experience in Adverse Event reporting, posting queries in clinical database and onsiteoffsite coordination, client interaction, and resource handling. Must be proficient in SAE Processing, Clinical research, medical terminologies, Clinical Data CRF review, Coding, FDAs CFR guidelines, ICHGCP guidelines, Oracle ARGUS ARISg safety databases, MedDRA, WHODD, Oracle Inform, Oracle RDC, eCRF and Paper CRF. Knowledge of different therapeutic areas including Respiratory, Infectious, Cardiovascular, Neurology and Oncology is required
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