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 authorizationsPrepare, review, and manage regulatory documentation within your area of expertiseReview and assess promotional materials and activities from a regulatory perspectiveAct as a point of contact on assigned projects, supporting client communication and regulatory discussionsContribute to project planning, timelines, and delivery of regulatory servicesCollaborate with senior regulatory colleagues who provide guidance and oversightStay 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 productsHands-on experience with product lifecycle management in a post-marketing settingExposure to regulatory review of promotional materials is highly valuedAbility to work independently while contributing effectively within a teamStrong communication skills, including written and spoken EnglishPrior client-facing experience is an advantage but not essentialBachelor’s or Master’s degree in Life Sciences or a related field

Ways of working

Hybrid working model with flexibilityMilan office preferred; candidates based in Northern Italy may be consideredOccasional 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.

The potential base pay range for this role, when annualized, is 39 700,00 € - 59 700,00 €. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.