Regulatory Affairs Consultant

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 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 g...