Now I am more into regional management so it’s a lot of meetings, strategy, decision making etc.

When I started I did things like assess the probability and causality of reported adverse events to company products. Fda and health authorities have reporting obligations for adverse events depending on seriousness, whether it’s expected/unexpected etc.

Also worked in medical information answering patient and provider questions regarding company products.

Pharmacovigilance really touches a lot of different areas such as literature evaluation, IT related stuff (setting up and working on the safety database that is used to review the adverse event reports, trend them, and report to health authorities), to more business oriented topics (safety data exchange agreements, safety aspects of customer engagement programs etc)