About the job

• Reviewing the published reports/biomedical literature to ascertain if they contain individual case reports and Non-individual case reports.
• Applying regulatory and internal guidance to determine if the article meets the definition of a valid case report and Non- individual case reports.
• Write accurate and concise summaries that capture the key elements from these published reports
• Ensure consistent coding of medical history, drugs and adverse event terms
• Evaluation of Serious Adverse Event to ensure accurate processing from source documents with emphasis on quality and timeliness
• Creating summary content in a range of formats (narrative summaries, structured database inputs, electronic formats for regulatory filing) to support the drug safety reporting and information requirements of pharma industry client
  

Qualifications

M.Pharm / B.Pharma / BAMS / BHMS / PhD./ Pharm D / BDS

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