Global Regulatory Affairs Lead
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 diseases. You will shepherd HA interactions, author regulatory documents, and ensure timely submissions while maintaining compliance.
The role requires 3–4 years in international regulatory affairs, with preferred experience in rare diseases. You will shepherd HA interactions, author regulatory documents, and ensure timely submissions while maintaining compliance.