Greater Melbourne Area
Daily responsibilities include evaluating, assessing and processing of potential and follow up adverse event case reports as per client procedure and through systems and processes designed to meet Good Pharmacovigilance (GPV) practice. Acts as part of the team to ensure project outcomes and KPIs are met.
Assisting in the provision of quality, up to date medical information to both healthcare professionals and consumers alike in a timely and satisfactory manner. Services a range of clients with varied product portfolios from OTC, prescription medicines, generics and medical devices and assisting in triaging of adverse drug report and product technical complaints for further follow up. Transition to Medical Information Junior Associate in October 2018