What are the responsibilities and job description for the Regulatory Affairs Consultant position at iqvia?
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 Stay up to date with evolving regulatory requirements and apply them in a practical, client-focused way 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 Milan office preferred; candidates based in Northern Italy may be considered 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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.