Role – Writer Role
Location – Pune
Education Qualification- Mpharm., Bpharm., pharmD
Experience- 6 months-1 Yrs.
Notice Period- Immediate -30 Days
Roles & Responsibilities:
Role & Responsibility
– 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.
Pharmacovigilance &DrugSafety;(Med Device
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