**Overview**
IQVIA is looking for a Regulatory Affairs Consultant to join our Regulatory Affairs & Pharmacovigilance team in Italy. This role will support a range of client projects focused on the lifecycle management of medicinal products, with opportunities to work on both local and international assignments.

You will join a small, experienced regulatory team and work closely with senior colleagues while managing your own responsibilities with a high level of autonomy.

Regulatory Affairs Consultant
Location: Italy (Hybrid – Milan office preferred)
Contract: Fixed-term (12 months)

**What you’ll do**

+ Support and lead regulatory activities related to the lifecycle management of medicinal products, including post-approval changes and maintenance of marketing authorizations
+ Prepare, review, and manage regulatory documentation within your area of expertise
+ Review and assess promotional materials and activities from a regulatory persp...