Eros Biasiolo

Eros Biasiolo has a diverse work experience in the pharmaceutical industry. Starting in 2010, they worked as a Medical Information Officer/ Specialist at Pfizer for two years. From 2012 to 2014, they held the position of Medical Information Specialist/Scientific Affairs Advisor at Celgene. In 2016, they worked as a Regulatory Affairs/Veeva Consultant for Merck Group. Eros continued their regulatory affairs work at Merck KGaA, Darmstadt, Germany from 2018 to 2019 as a Regulatory Affairs/Veeva/RIMS Consultant. In 2019, they joined Health Unlimited as a Senior Medical Writer and stayed until 2020. From 2020 to 2021, Eros worked at Norgine as a Senior Central Medical Affairs Executive on an interim basis. In 2021, they became the Compliance and Sustainability Manager at Aspire Pharma Ltd, overseeing compliance responsibilities and managing the sales team. Currently, they work as the Lead Medical Reviewer at Indegene, starting in November 2021. Throughout their career, Eros has also operated their own consultancy, EBiassiolo Limited, as a Senior Medical Affairs/Regulatory Affairs Consultant and Project Manager from 2013 to 2020.

Eros Biasiolo has a degree in Pharmacy from the Università degli Studi di Padova. The specific years of study and completion are not provided.