Global Rare Disease Regulatory Affairs Specialist

IQVIA Italia, on behalf of Chiesi Farmaceutici, seeks a Global Rare Disease Regulatory Affairs Specialist for EU and international submissions in a multinational context. The role focuses on preparing regulatory documents, coordinating regional filings, and ensuring quality submissions within timelines.The ideal candidate has 2–3 years in EU/INT regulatory...

Overview In this role you will support Chiesi’s Global Rare Diseases portfolio by managing CMC regulatory activities across submissions and lifecycle. You will collaborate with Core teams, GCST, and external CMOs to ensure compliance and timely regulatory deliverables. You will influence regulatory strategy and lead documentation for marketing...

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...

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...

IQVIA on behalf of Chiesi Farmaceutici seeks a Global Regulatory Affairs Manager to join our international team for a fixed-term maternity cover. Based in Italy, you will partner with GRL and GRT to shape regulatory strategies across EU and global markets.The role requires 3–4 years in international regulatory affairs, with preferred experience in rare...

Chiesi seeks a Regulatory Affairs (RA) Senior Manager with strong CMC pre/post-approval experience to support the Global Rare Diseases portfolio. You will lead CMC documentation, author sections, and advise on regulatory strategies across global submissions.The role emphasizes collaboration with cross-functional teams, external CMOs, and continuous learning...

Global Regulatory Affairs Manager-Maternity Cover IQVIA Italia•Emilia-Romagna, Italy 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 Regulatory Affairs Manager (fixed-term maternity...

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.Main...

Global Regulatory Affairs Manager-Maternity Cover IQVIA Italia•Emilia-Romagna, ItalyPossiede le competenze per ricoprire questo ruolo? Legga i dettagli completi qui sotto e invii la sua candidatura oggi stesso.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...