Pharmacovigilance Associate at Teva

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

How you’ll spend your day

  • Processing adverse events reports from post marketing sources into Teva’s global safety database.
  • The different sources / types of reports includes 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 global environment: Interacting with other global PhV units and local PhV reps. around the world.

Your experience and qualifications:

  • Freshers
  • M. Pharm
  • Location: Bangalore, India, 560052
  • Job Id: 56869
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