Help Keep Essential Medicines Available To Patients At IQVIA, our Regulatory Affairs teams help pharmaceutical clients navigate regulatory requirements and maintain medicinal products on the market. We are looking for a Regulatory Affairs Analyst to join our team in Italy. This is an opportunity for an early-career regulatory professional to build broader experience across medicinal-product lifecycle activities, regulatory submissions and client support while working alongside experienced Regulatory Affairs colleagues.

Contract: Fixed-term maternity cover Support the regulatory lifecycle management of medicinal products on the Italian market. Support submissions and routine communications with Italian health authorities. Assist with lifecycle maintenance, marketing authorisation transfers, labelling, CMC activities and other regulatory procedures, depending on project requirements.

Support activities connected with promotional materials and ongoing product maintenance. Track deliverables, timelines and priorities across several concurrent projects. Work closely with senior Regulatory Affairs colleagues, escalating risks or more complex matters when necessary.

A bachelor’s or master’s degree in pharmacy, biology, biotechnology or another relevant life-sciences discipline. Approximately two years of relevant Regulatory Affairs experience. Practical experience supporting operational regulatory activities for medicinal products.

Previous experience in a pharmaceutical company, CRO, consultancy or similar regulated environment. Understanding of the Italian regulatory environment and medicinal-product lifecycle activities.

Experience preparing or coordinating regulatory documentation and submissions. Strong planning and organisational skills, with the ability to prioritise activities against different client and authority deadlines. Good written and verbal communication skills. Confidence using Microsoft Office and relevant regulatory systems or publishing tools.

Fluent





Italian and professional working proficiency in English. You will join a collaborative Regulatory Affairs environment where you can develop your expertise through exposure to different clients, products and regulatory activities. You will be supported by experienced colleagues while having meaningful ownership of day-to-day deliverables and client interactions.

This role offers the opportunity to strengthen your knowledge of the Italian regulatory landscape, broaden your lifecycle-management experience and contribute directly to keeping medicinal products compliant and available to patients. This is a hybrid position, combining remote working with attendance at the office for face-to-face collaboration. The position is offered as fixed-term maternity cover.

The exact duration will be aligned with the employee’s effective period of absence, in accordance with applicable Italian requirements. 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.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. 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. The potential base pay range for this role, when annualized, is 33 000,00 € - 49 400,00 €.

The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; and/or schedule (full or tempo parziale). 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.

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