Global Rare Disease Regulatory Affairs Specialist EU

21 ore fa

Gallicano Nel Lazio, Lazio, Italia LinkedIn Tempo pieno

IQVIA, on behalf of Chiesi Farmaceutici, is seeking a Global Rare Disease Regulatory Affairs Specialist EU&INT to join our international team in Rome, Italy.

The role involves preparing regulatory documents for submissions, coordinating with consultants and affiliates, reviewing submission documents, and guiding colleagues. xysqume

Controlli attentamente tutta la documentazione richiesta per la candidatura prima di fare clic sul pulsante apposito in fondo a questa descrizione.

2-3 years in EU/INT regulatory affairs, lifecycle management experience, and fluent English are required.