Home / job / Regulatory Affairs Consultant

Regulatory Affairs Consultant

IQVIA · Milan, Lombardy, Italy

Location
Milan
Job Type
Full time
Posted
June 29, 2026

Job Description

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 ...

    • Ready to Apply?

    Submit your application for Regulatory Affairs Consultant at IQVIA

    Apply Now