21 set - Milano
Iqvia
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.
Dato l'elevato interesse per questa posizione, la preghiamo di candidarsi tempestivamente se il suo profilo è in linea con il ruolo.
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. You will take ownership of routine operational activities, interact with clients and health authorities, and help ensure that regulatory deliverables are completed accurately and on time.
Contract: Fixed-term maternity cover
What you will do
- 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.
What will help you succeed
- A bachelor’s or master’s degree in pharmacy, biology, biote
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