IQVIA Italia is looking for RSU interns based in Milan to join our multi-sponsor RSU team.
This person will support senior members of the team in the Start-Up process of clinical studies
Main Accountabilities
Support Regulatory , Start-Up and Maintenance activities according to applicable regulations, SOPs and work instructions
Prepare site regulatory documents , reviewing for completeness and accuracy
Ensure contracts are fully executed, regulatory documents and approvals are granted, and specific project deliverables are completed
Review, establish and agree on project planning and project timelines
Requirements
MSc degree with strong record of academic achievement in Life Science field (Pharmacy, CTF, Biology, Chemistry etc.)
Previous experience as Data Manager / Study Coordinator, having managed direct contact with Hospital Ethical Committees would be considered a plus
Proficiency both in English (written and spoken) and Italian
Excellent Microsoft Office Skills
Good communication skills
Ability to be multi-tasking in a fast-paced environment and to work on a team
At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world.
The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our ,+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way.
