European Medicines Agency
The Human Medicines Division oversees and manages human medicines throughout their lifecycle, from evidence generation planning, through evaluation and monitoring of medicines to interfacing with stakeholders to facilitate access and optimal use. The division also supports the European regulatory network to produce patient-centred high-quality scientific opinions. In this role, you will provide administrative, regulatory and scientific support to the safety, efficacy or quality aspects of human medicines throughout their lifecycle, ensuring consistent outputs of high quality in the context of pre and post authorisation activities. This selection procedure aims to create a reserve list for a variety of different positions across the Agency, from product coordinator, to committee support assistant, to procedure manager for minor procedures or validation officer, generally involving the management and preparation of documentation related to the evaluation of medicines. On a daily basis, you will be cooperating with highly qualified professionals from from 30 EU and EEA countries.
Lees hier meer…
Om op deze vacature te solliciteren bezoek je nl.whatjobs.com.