1. Receive information on adverse events, perform initial checks, search database to prevent duplicate entries, create case file and initialize received drug safety reports in the DS&E tracking tool and/or safety database. 2. Ensure scientific rigor through accurate, complete and consistent data entry of adverse event reports from source documents with emphasis on timeliness and quality. 3. Evaluate and finish processing of non-expeditable AE reports, including review for completeness and ...
Novartis - 4 months ago
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Safety Processing Expert diverse, talented and performance driven people. All of which makes us one of the most rewarding employers -
Hyderabad, Andhra Pradesh Naukri.com - 24 days ago
