Country Regulatory Submissions Specialist

Work ScheduleControlli attentamente tutta la documentazione richiesta per la candidatura prima di fare clic sul pulsante apposito in fondo a questa descrizione.Standard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin us as a Country Approval Specialist and make an impact at the forefront of innovation. We have successfully supported the top 50...

IQVIA, on behalf of Chiesi Farmaceutici, is seeking a Global Rare Disease Regulatory Affairs Specialist for EU and INT in Rome, Italy. The role supports submissions to regulatory authorities and lifecycle management for global rare disease products, collaborating with consultants, partners, and affiliates.Requirements include 2–3 years in 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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed...

OverviewSe pensa di essere il profilo ideale per la seguente opportunità, si candidi dopo aver letto la descrizione completa.In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina's medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to...

Thermo Fisher Scientific is seeking a Principal Regulatory Affairs Specialist to join our global Regulatory Affairs team. You will lead regulatory strategies for Phase 1–4 trials, coordinate global submissions and interact with sponsors and clients to ensure compliant deliverables.Based in Rome, this full-time role offers a chance to impact trials...

Novo Nordisk A/S in Italy is seeking a Senior Study Start-up Specialist to drive regulatory submissions and site activation for clinical trials, ensuring compliance with ICH-GCP and local requirements. You will manage end-to-end start-up, coordinate with internal and external stakeholders, maintain trial master file, and support contracts and budgets in a...

Novo Nordisk A/S in Italy is seeking a Senior Study Start-up Specialist to drive regulatory submissions and site activation for clinical trials, ensuring compliance with ICH-GCP and local requirements. You will manage end-to-end start-up, coordinate with internal and external stakeholders, maintain trial master file, and support contracts and budgets in a...

Novo Nordisk A/S in Italy is seeking a Senior Study Start-up Specialist to drive regulatory submissions and site activation for clinical trials, ensuring compliance with ICH-GCP and local requirements. You will manage end-to-end start-up, coordinate with internal and external stakeholders, maintain trial master file, and support contracts and budgets in a...