Global Regulatory Affairs Manager: CTA Submissions

Work ScheduleLe seguenti informazioni forniscono una panoramica delle competenze, delle qualità e delle qualifiche necessarie per questo ruolo.Standard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific, you'll discover meaningful work that

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...

Drive the regulatory strategy, planning and execution across key regions for the assigned development pipeline projects (from early preclinical phases)Collaborate with cross-functional teams to ensure timely submissions, approvals, and compliance with global regulatory requirements, supporting the successful development and registration of innovative...

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...

Angelini Pharma is seeking a Senior Manager, Global Regulatory Strategy in Rome to drive regulatory strategy across key regions for the development pipeline. You will collaborate with R&D, Clinical Development, CMC, Safety and Quality to ensure timely submissions and approvals.You will monitor evolving regulatory requirements (FDA, EMA, ICH) and lead...

About usChiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we...

Overview In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional input for regulatory dossiers. The position emphasizes collaboration across...

IQVIA Italia is seeking a Global Regulatory Affairs Manager (maternity cover) to join an international team in Rome, Italy. The role supports EU and global regulatory strategy and ensures timely submissions across regions.Requirements include 3–4 years in international regulatory affairs, a Master's degree, and fluent English, with strong organizational...

Job DescriptionL'esperienza richiesta ai candidati, così come le competenze e le qualifiche aggiuntive necessarie per questo lavoro, sono elencate di seguito.We are seeking aRegulatory Business Partnerto support the growth and delivery of consulting services within our Regulatory Consulting business unit for Life Sciences clients.This role acts as a bridge...