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