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Teva Pharmaceuticals is hiring for Medical Writers who can fulfill the following requirement

Job Location: Mumbai
Years of experience:3-6

Roles & Responsibilities:

Processing adverse events reported from post-marketing sources into Teva's global safety database

The different sources/types of reports include: Reports from the scientific literature, Teva partners (other pharmaceutical companies), Health Authorities, Non-interventional studies, and other programs

The processing includes Adverse Events coding (in medical dictionary - 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 PhV units and local PhV reps. around the world

Taking part in the development and maintenance of an efficient and robust Pharmacovigilance system

If your profile matches the above requirement, please share your updated resume to [email protected] with the subject line as "Medical Writer"
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