How You’ll Spend Your Day:
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- Processing adverse event reports from post-marketing sources into Teva’s global safety database.
- Handling different sources/types of reports including those from scientific literature, Teva partners (other pharmaceutical companies), Health Authorities, Non-interventional studies, and other programs.
- Performing adverse events coding (using MedDRA), drug coding in the Company Product Dictionary, seriousness and labeling assessment, and submission to health authorities.
- Working in a global environment: Interacting with other global Pharmacovigilance units and local Pharmacovigilance representatives around the world.
Your Experience and Qualifications:
- M.Pharm degree
- Freshers are welcome to apply
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