Matteo Barion

Background

About Matteo Barion

I'm a Global Pharmacovigilance Operations Specialist with experience in the management of Serious Adverse Event occurred in international clinical trials and Individual Case Safety Reports occurred in post-marketing, from case intake to submission to the relevant Health Authorities (EMA, FDA and Health Canada). Moreover, I have experience on management of service providers, writing Standa Operationg Procedures and inspection from Health Authoririties. In the clinical research environment I've worked also as Clinical Data Manager and I've improved the abilities to collect and manage of data of international clinical trials in different phases and therapeutics area. In these years I've increased the ability to work an an international environment with also an experience of 4 months of work in Denmark and I've worked also in pharmaceutical industries as consultant. I like the clinical research and to share my experience in the events of professional associations and university. Specialties: Pharmacovigilance, Reconciliation of SAE/ICSRs, Submission of SUSAR/ICSRs to Health Authorities, Clinical Coding (MedDRA and WHO-DD), Oracle AERS, Oracle ARGUS, Data Management, CDASH, Query Management, Laboratory Mangement, external data management, Oracle Clinical, EDC software (Oracle RDC, Datatrak, Inform and Cmed), Chromatographic analytical methods, Chemistry and Pharmaceutical technologies.