Pharmacovigilance and Medical Information Jobs in Italy

Provide expert advice on GVP compliance and regulatory matters, acting as quality partner to PV Operations (US/DK) and the EU QPPV. Author and maintain GVP Quality procedures and support implementation of new or updated GVP requirements.

Ensure the creation of high quality medical information content in a consistent and unbiased manner, while adhering to all applicable rules, regulations and SOPs. Develop and maintain material such as (Non)Standard Response Letters and Frequently Asked

Act as key point of contact for TPM on all operational aspects - equipment, performance, cycle time, yield etc. Build solid relationships with first tier TPM’s and drug linker TPM’s to monitor manufacturing performance weekly through the application

Responsible to streamline and accelerate growth in Italy in the field of Solid organ transplantation (SOT) focusing on our MDR granted indications of lung transplantation (LuTX) and heart transplantation (HTX). Selling clinical data, ensure cross organ