Senior CMC Regulatory Affairs Manager Global Rare Diseases

Overview In this Senior Manager CMC Regulatory Affairs role, you drive global CMC submissions for Chiesi Global Rare Diseases, shaping regulatory strategies and interactions with authorities. You work cross-functionally with CMOs and internal teams to assemble documentation, respond to questions, and ensure timely, high-quality filings. You’ll influence...

Select how often (in days) to receive an alert:Senior Manager, CMC Regulatory Affairs, Global Rare DiseasesDate: 1 Oct 2026Department: GRD Regulatory AffairsBusiness Area: R&D, Pharmacovigilance & Regulatory AffairsJob Type: Direct EmployeeContract Type: PermanentLocation: Parma or Chiesi Affiliates in , ITAbout usChiesi is an international research-focused...

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...

Questa posizione è in Chiesi GroupRiassunto dell'opportunità da parte della Joinrs AI:Chiesi Group ricerca un Principal Regulatory Writer con laurea in scienze della vita o affini per gestire e sviluppare documenti regolatori in ambito farmaceutico per malattie rare. Il candidato contribuirà a sottomissioni globali collaborando con team multidisciplinari....

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...

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 cover) to join an exciting working environment in a dynamic and international...

Real World Evidence Lead Endo-Metabolic, Global Rare Diseases Date: 22 Jul 2026 Department: GRD Global Medical Affairs Business Area: Mktg, Market Access, Bus. Excellence & Med. Affair Job Type: Direct Employee Contract Type: Permanent Location: Europe, IT About us Chiesi is an international research-focused biopharmaceutical group with 90 years’...

Overview In this role you drive the global Real World Evidence (RWE) strategy for the Endo-Met portfolio, aligning evidence plans with research and commercial goals. You lead cross-functional execution, shaping partnerships and data sourcing to inform regulatory, payer, and clinical decisions. You’ll advance innovative methodologies and publish impactful...

Select how often (in days) to receive an alert: Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy....