ICON is a integral healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a Regulatory Technician you will work with the Clinical Trials Information System (CTIS), and will also provide support for submissions and other documents by performing necessary tasks including assembly, dispatch among others and coordinating resources for submissions, Proactively identify and mitigate risks through CTIS helpdesks regarding data/document management and upload to CTIS and liaise with internal/external stakeholders to resolve Actively maintain applicable study-level account access for assigned projects for CTIS to maintain compliance and confidentiality Collaborate with key stakeholders to manage and perform data entry and document upload Perform Quality Control review in accordance with applicable process Ensure project-specific training is completed on time, as applicable Mandatory advanced English (speak,



read, write) Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. A range of health insurance offerings to suit you and your family's needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well‑being. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

📌 It Technician Service Desk (Barcelona)
🏢 FUNDACIO INSTITU DE RECERCA EN ENERGIA DE CATALUNYA
📍 Barcelona