MBBS Pharmacovigilance Associate at Teva! MD Apply Online

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.

As Lead PV Professional, Medical Reviewer/Clinical Assessor within the ICSR operations sub-function within Patient Safety Operations (PSO), the role in the Global Patient Safety & Pharmacovigilance department within Teva Global R&D (Research & Development) reports to the Head of ICSR Operations.

Perform medical review and clarification of Trial related (AE’s) & Post marketing Adverse Evets (ADR’s) including narrative content, queries, coding for events and lab reports, expectedness, seriousness, causality, labelling and medical assessment comments as applicable.

Qualification – MBBS OR MD

Experience – Clinical medical experience of about 1-2 years and PV experience of at least 1 year as medical safety reviewer is recommended so as to fulfill the job role technical requirements on medical judgments.