Milan, Italy | Tempo pieno | Hybrid | R1536613 **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 perspective
- Act as a point of contact on assigned projects, supporting client communication and regulatory discussions
- Contribute to project planning, timelines,



and delivery of regulatory services
- Collaborate with senior regulatory colleagues who provide guidance and oversight **What we’re looking for**
- Experience in Regulatory Affairs with a focus on medicinal products
- Hands-on experience with product lifecycle management in a post-marketing setting
- Exposure to regulatory review of promotional materials is highly valued
- Ability to work independently while contributing effectively within a team
- Strong communication skills, including written and spoken English
- Prior client-facing experience is an advantage but not essential
- Bachelor’s or Master’s degree in Life Sciences or a related field **Ways of working**
- Hybrid working model with flexibility
- Occasional office presence expected **Why IQVIA** IQVIA is a global leader in advanced analytics, technology solutions and clinical research services. We work at the intersection of data, science and healthcare to help clients accelerate innovation and improve patient outcomes worldwide.

📌 Regulatory Affairs Consultant (Milano)
🏢 Iqvia
📍 Milano