Life Sciences Internship at IQVIA, Italy | Earn €900 Per Month | Apply Now
If you are a Life Sciences Master’s graduate or a clinical study coordinator looking to transition into international clinical trial operations, this position within the Country Site Activation team at IQVIA Italy is an exceptional entry point. Based in the corporate hub of Milan, this role serves as a launchpad for navigating ethics committee submissions and trial start-up procedures. For detail-oriented graduates searching for a high-value Life Sciences Internship, this opportunity offers active, hands-on exposure to regulatory tracking and clinical documentation. It provides a direct path to building a long-term, rewarding IQVIA career and stands out as a premier selection for anyone tracking a competitive Internship in Italy within the biopharmaceutical sector.
- Position: Internship – Country Site Activation, Milan
- Location: Milan, Italy
- Job ID: R1519115
About The Company
IQVIA is a world-renowned, leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. Powered by advanced data analytics and clinical expertise, IQVIA creates intelligent connections that accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes worldwide.
The Country Site Activation Team functions as a high-compliance engine responsible for securing the documentation, licenses, and ethics clearances required to activate experimental clinical trial sites. Entering this specialized business unit means moving past theoretical science and taking active, structural part in the regulatory mechanisms that govern localized study activations across Italy.
Life Sciences Internship – Key Responsibilities
The Site Activation Intern acts as a vital supporting asset, assisting senior specialists in processing documentation pipelines to achieve rapid site greenlight status.
Your core regulatory support, document auditing, and milestone tracking duties include:
- Dossier Preparation Assistance: Supporting the team in compiling, preparing, and tracking local regulatory and site submission dossiers required for clinical trials in Italy.
- Essential Document Filing: Assisting with core study start-up milestones, including organizing, checking, and filing critical documentation within the electronic Trial Master File (eTMF).
- Timeline Optimization: Tracking and following up on site activation milestones, documentation deadlines, and activation target dates to advance this Life Sciences Internship.
- Regulatory Landscape Mapping: Gaining functional exposure to Italian regulatory requirements, National AIFA decrees, and localized Ethics Committee (CE) processes.
- Cross-Functional Collaboration: Partnering with data management, clinical monitoring, and internal project teams to support broader operational activities and process improvement initiatives for this Internship in Italy.
Qualifications & Profile Requirements For Life Sciences Internship
This corporate internship is meticulously optimized for highly structured, analytical candidates who possess a deep interest in clinical trial regulatory affairs.
- Mandatory Academic Criteria:
- Educational Foundation: A completed, formal Master’s Degree in a Life Science discipline (e.g., Biotechnology, Biology,) is required for this position to kickstart a rewarding IQVIA career.
- Desirable Skills & Experience:
- Any prior exposure or academic specialization in Regulatory Affairs or Study Start-Up (SSU) activities is a significant plus.
- Prior experience operating as a clinical Study Coordinator with exposure to Regulatory and Start-Up workflows.
- Fluent written and verbal communication skills in English, paired with full professional proficiency in Italian to handle regional regulatory documentation.
- Solid digital literacy, with high attention to detail and an organized approach to data management.
Logistics, Regulatory Conditions & Stipend
- Location: Milan, Italy.
- Workspace Framework: Hybrid Model (Requiring 2 to 5 days per week of on-site presence at the Milan office, scaled based on ongoing business and project tasks).
- Employment Status: Full-Time Intern.
- Job Requisition ID: R1519115.
- Legal Framework & Allowance: The contract is governed by the official Regione Lombardia internship conditions, providing a fixed gross reimbursement of €900.00 per month for the internship duration.
- Annualized Reference Range: The standard full-time annualized baseline value for equivalent career trajectories tracks between €25,500.00 and €38,300.00.
In short, the Country Site Activation Internship at IQVIA is a definitive route to transitioning your scientific Master’s degree into a highly sought-after clinical operations asset. Securing an appointment here allows you to bypass general lab work and take active, structural part in the ethics submissions, regulatory dossiers, and tracking tools that bring breakthrough clinical therapies safely to reality. If you reside in or can commute to Milan, hold the mandatory life sciences master’s degree, and possess an compromise-free commitment to data precision, apply today to secure this premier Life Sciences Internship, launch an exceptional IQVIA career, and lock in this outstanding Internship in Italy.
