Regulatory Affairs Job at IQVIA Italy | Life Sciences Candidates, Apply Online
A rare chance for early-career regulatory professionals has emerged at IQVIA in Milan, Italy. This full-time, hybrid Regulatory Affairs Job offers an opportunity to gain experience across regulatory submissions and client support in the pharmaceutical sector. Interested candidates are encouraged to apply promptly.
- Job Position: Regulatory Affairs Analyst
- Location: Milan, Italy
- Reference Number: R155551
About The Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The organization focuses on creating intelligent connections to accelerate the development and commercialization of innovative medical treatments, ultimately improving patient outcomes and population health worldwide.
Regulatory Affairs Job Description
The Regulatory Affairs Job as an Analyst will support pharmaceutical clients in navigating regulatory requirements and maintaining medicinal products on the market. This role involves taking ownership of routine operational activities, interacting with clients and health authorities, and ensuring that regulatory deliverables are completed accurately and on time.
Key Responsibilities
- Support the regulatory lifecycle management of medicinal products on the Italian market.
- Prepare, review and coordinate regulatory documentation and submissions.
- Support submissions and routine communications with Italian health authorities.
- Work with clients to understand requests, coordinate activities and meet regulatory and contractual deadlines.
- 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.
- Participate in internal and client meetings and communicate progress clearly.
- Follow applicable procedures and quality standards while contributing ideas for practical process improvements.
Eligibility Criteria
- A bachelor’s or master’s degree in 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.
- Confidence communicating with clients, internal stakeholders and, ideally, health authorities.
- Strong planning and organisational skills, with the ability to prioritise activities against different client and authority deadlines.
- Good written and verbal communication skills.
- Strong attention to detail and the ability to follow established procedures consistently.
- Confidence using Microsoft Office and relevant regulatory systems or publishing tools.
- Fluent Italian and professional working proficiency in English.
Why Join IQVIA?
Joining IQVIA offers a collaborative Regulatory Affairs environment where professionals can develop their expertise through exposure to different clients, products, and regulatory activities. Employees will be supported by experienced colleagues while having meaningful ownership of day-to-day deliverables and client interactions, strengthening their knowledge of the Italian regulatory landscape.
This Regulatory Affairs Job opportunity at IQVIA for a Regulatory Affairs Analyst is ideal for early-career professionals looking to enhance their regulatory expertise and contribute to the healthcare sector. Interested candidates should apply before the deadline to secure their chance to be part of this impactful organization.
