Global Rare Disease Regulatory Specialist EU&INT

IQVIA, on behalf of Chiesi Farmaceutici, is seeking a Global Rare Disease Regulatory Affairs Specialist for EU and INT in Rome, Italy.Per il seguente ruolo potrebbero essere richieste diverse soft skill ed esperienze. La preghiamo di consultare attentamente la panoramica riportata di seguito.The role supports submissions to regulatory authorities and...

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...

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. 2-3 years in EU/INT regulatory...

On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for this global, rare disease regulatory affairs specialist in EU and INT to join an exciting working environment in a dynamic and international...

On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for this global, rare disease regulatory affairs specialist in EU and INT to join an exciting working environment in a dynamic and international...

On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a Global Rare Disease Regulatory Affairs Specialist EU&INT to join an exciting working environment in a dynamic and international atmosphere.Vuole...

Alfasigma is seeking a Regulatory Affairs Specialist to manage local Italian product regulatory activities for Rx and OTC lines. You will prepare and submit dossiers, variations, and renewals while maintaining high data quality and regulatory compliance. You will collaborate with Quality, Medical Affairs, Market Access and Regulatory teams to navigate...

Alfasigma is seeking a Regulatory Affairs Specialist to manage local Italian product regulatory activities for Rx and OTC lines. La preghiamo di leggere attentamente le informazioni contenute in questo annuncio di lavoro per comprendere esattamente cosa ci si aspetta dai potenziali candidati. You will prepare and submit dossiers, variations, and renewals

Drive the regulatory strategy, planning and execution across key regions for the assigned development pipeline projects (from early preclinical phases) Scopra di più su questo ruolo leggendo le informazioni qui sotto, quindi invii la sua candidatura per essere preso/a in considerazione. Collaborate with cross-functional teams to ensure