Internship: Regulatory Affairs Intern, Italy, 2025
Internship: Regulatory Affairs Intern, Italy, 2025
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Job Description
Posting Title: Internship: Regulatory Affairs Intern Italy 2025
Help us get ahead of disease together with our Internship in the Regulatory team 2025!
Education required: BS/MSc degree in in a scientific (technical biological chemical pharmacological) or health related discipline and/or Regulatory Affairs with a strong interest and knowledge of Regulatory procedures
Other requirements: Must be enrolled at the University in Italy for the duration of your program/ Creditbearing internship is preferred (SG)
Language requirement: Written and spoken fluency in English Italian knowledge is a plus
Expected Start date: July 2025
Internship period: 6 months
Application deadline: 22 of May 2025 We recommend you apply as soon as possible. We will close this vacancy when we have enough applications so please apply as soon as you can so your application can be considered.
Internship Type: Curricular 100% onsite
Are you looking to gain valuable world work experience and help to positively impact the health of billions of people Apply for a GSK Internship today!
A GSK internship offers you the opportunity to kickstart your career to take on a real role with genuine impact! Youll take on challenging serious work on live projects or assignments. Youll also get to learn from us develop your skills and gain valuable experience for wherever the future takes you.
What will you do
The Regulatory Team in the GSK Global Health R&D unit (GSK Vaccine Institute for Global HealthGVGH) is responsible for the regulatory strategy for the development of new vaccine candidates and for the preparation and maintenance of regulatory documentation needed to conduct Clinical Trials in the countries of interest for the candidate vaccines developed by the institute.
The team is responsible for
Elaborating the regulatory strategy for the development of new candidate vaccines
Providing regulatory advice to all Institute functions as needed
the preparation of regulatory documentation needed for clinical trial applications in the countries of interest according to local regulations
Supporting the Clinical Departments Clinical sites in the interactions with regulatory authorities
Documents life cycle management and archiving
Clinical trial submission documentation maintenance throughout clinical development
What will you learn (Optional/Compulsory for SG)
The intern will understand the role of Regulatory Affairs in the early phases of the clinical development of a new vaccine and the interconnections between the different functions contributing to the clinical development of a vaccine. The intern will also get familiar with local and global regulations governing the development of a new medicinal product and in particular of Vaccines. The required support will progressively increase both in the autonomy of task execution and in the overall vision of the department and the organization. The intern will support the following activities:
Analysis of local regulations
Preparation of regulatory documentation in particular administrative and quality documentation relative to the candidate vaccine Drug Substances and Drug Products
Copywrite clearance of Literature references included in regulatory submissions
Document archiving
Project/clinical trial meetings attendance
What are we looking for
A lively interest in the biopharma industry
Adaptability to change and working under pressure
Excellent communication skills
Strong problemsolving skills driven by curiosity
Drive and confidence to trust your own judgment
Proactive ambitious nature with interest to learn quickly
What do we offer you
Reimbursement of 500 euro per month lunches at the Company canteen
Lets do this!
Youll find hints tips and guidance on our recruitment process on our website
Learn more about the application process now!
Need help with your application
Please email us at and let us know how we can help you.
Why GSK
Uniting science technology and talent to get ahead of disease together.
GSK is a global biopharma company with a special purpose to unite science technology and talent to get ahead of disease together so we can positively impact the health of billions of people and deliver stronger more sustainable shareholder returns as an organisation where people can thrive. We prevent and treat disease with vaccines specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies investing in four core therapeutic areas (infectious diseases HIV respiratory/ immunology and oncology).
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders its also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired encouraged and challenged to be the best they can be. A place where they can be themselves feeling welcome valued and included. Where they can keep growing and look after their wellbeing. So if you share our ambition join us at this exciting moment in our journey to get Ahead Together.
If you require an accommodation or other assistance to apply for a job at GSK please contact the GSK Service Centre at(US Toll Free) or 1 (outside US).
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race color religion sex (including pregnancy gender identity and sexual orientation) parental status national origin age disability genetic information (including family medical history) military service or any basis prohibited under federal state or local law.
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GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSKs commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
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Required Experience:
Intern
Employment Type
Full-Time
