CTR Regulatory Specialist — Italy

PSI is seeking a regulatory submissions specialist in the Milan area to facilitate start-up activities for clinical studies under the EU CTR framework. The role involves coordinating Italy CTR Part II submissions, communicating with authorities, project teams and vendors, and ensuring accurate document translations.The candidate should have a scientific...

PSI is seeking a regulatory submissions specialist in the Milan area to facilitate start-up activities for clinical studies under the EU CTR framework. The role involves coordinating Italy CTR Part II submissions, communicating with authorities, project teams and vendors, and ensuring accurate document translations.The candidate should have a scientific...

PSI is seeking a regulatory submissions specialist in the Milan area to facilitate start-up activities for clinical studies under the EU CTR framework. The role involves coordinating Italy CTR Part II submissions, communicating with authorities, project teams and vendors, and ensuring accurate document translations.The candidate should have a scientific...

PSI is seeking a regulatory submissions specialist in the Milan area to facilitate start-up activities for clinical studies under the EU CTR framework. The role involves coordinating Italy CTR Part II submissions, communicating with authorities, project teams and vendors, and ensuring accurate document translations.The candidate should have a scientific...

PSI is seeking a regulatory submissions specialist in the Milan area to facilitate start-up activities for clinical studies under the EU CTR framework. The role involves coordinating Italy CTR Part II submissions, communicating with authorities, project teams and vendors, and ensuring accurate document translations.The candidate should have a scientific...

PSI is seeking a regulatory submissions specialist in the Milan area to facilitate start-up activities for clinical studies under the EU CTR framework. The role involves coordinating Italy CTR Part II submissions, communicating with authorities, project teams and vendors, and ensuring accurate document translations.The candidate should have a scientific...

JSB Solutions cerca una figura di Regulatory Affairs Specialist Italia da inserire nella divisione Regulatory Affairs. Il ruolo comporta attività regolatorie nazionali ed EU e gestione dossier, con focus su conformità e supporto agli audit.Sede principale a Milano, possibilità di esprimere preferenze tra sedi italiane. L'offerta prevede formazione,...

Overview As an RSU Specialist, you will lead country-specific site activation and regulatory activities within IQVIA's FSP team in Italy. You will act as the primary liaison for investigative sites and project teams, ensuring compliant, timely site activation and regulatory documentation. You will leverage local regulatory expertise to support timelines,...

DEADLINE EXPIREDDeadline for applying: October 31, 2023 Description PROFILE: The resource will deal with the analysis of the content of the Authority’s provisions, also for aspects relating to the evolution of the regulatory context within the EU, ensuring the relevant communication within the company, ensuring their correct interpretation and supporting...