Ctr Regulatory Specialist — Italy

Psi CRO is seeking a Regulatory Submissions Specialist to drive CTR Part II submissions for Italy under the EU CTR. The role collaborates with regulatory and ethics teams to coordinate packages, communicate with authorities, and ensure timely, compliant documentation in a hybrid setup near Milan.You will review translations, track documentation flow, and...

Sun Chemical, based near Milan in Italy, seeks a Specialist Safety Product to manage documentation for product safety and regulatory labeling. The role interfaces with the EMEA Regulatory Affairs team and production units to ensure accurate hazard labeling and up-to-date safety data sheets for customers.You will contribute to compliance with Italian laws and...

E.VA. Energie Valsabbia cerca un Permitting Specialist per gestire le autorizzazioni di progetti rinnovabili. Richiesta laurea e almeno 3 anni di esperienza, con conoscenza delle normative e dei software tecnici. L'inserimento è a tempo indeterminato, orario giornaliero dal lunedì al venerdì, sede Botticino (BS), Italia.Il ruolo prevede formazione...

Società farmaceutica cerca un esperto Affari Regolatori a Milano con 5-10 anni di esperienza, laurea scientifica, per gestire attività regolatorie e preparare dossier.

Psi CRO is seeking a Regulatory Submissions Specialist to drive CTR Part II submissions for Italy under the EU CTR. The role collaborates with regulatory and ethics teams to coordinate packages, communicate with authorities, and ensure timely, compliant documentation in a hybrid setup near Milan.You will review translations, track documentation flow, and...

In this role you drive regulatory submissions for Italy under the EU CTR, supporting the startup of studies for novel medicines. You will work within regulatory and ethics teams to coordinate packages, communicate with authorities, and ensure timely, compliant documentation. The position blends regulatory expertise with cross‑functional teamwork in a...

Location: Remote - EuropeLa preghiamo di verificare di possedere il livello di esperienza e le qualifiche adeguate leggendo la panoramica completa di questa opportunità qui sotto.Company: VB SpineVB Spine is expanding its European organization, and we are now finalizing recruitment for our main Regulatory Affairs team. The core team is based in Warsaw,...

In this role you drive regulatory submissions for Italy under the EU CTR, supporting the startup of studies for novel medicines. You will work within regulatory and ethics teams to coordinate packages, communicate with authorities, and ensure timely, compliant documentation. The position blends regulatory expertise with cross‑functional teamwork in a...

OverviewAs 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, risk...