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B-708 | Global Clinical Trial Assistant
hace 3 meses
.Detalles del empleoTipo de empleo: Contrato indefinidoUbicación: En remotoBeneficios:Abono gimnasioDescripción completa del empleo:As a Clinical Trial Assistant, you will be dedicated to one of our global pharmaceutical client sponsors with whom ICON shares a culture of innovation, flexibility, and a common vision of bringing life-improving drugs to market. Leading by example, you can set the standard of excellence and enjoy a challenging career in our exclusive programs.The Clinical Trial Assistant assists in the coordination and administration of the study activities from the start-up to execution and close-out, and within the Study Team to ensure quality and consistency of interventional study deliverables to time, cost, and quality objectives. As a Clinical Trial Assistant, you will have the opportunity to experience the full lifecycle of a project and genuinely contribute to drug development and improving patients' lives.What you will be doing:Trial Master File (TMF) creation and managementCo-ordinate entry and maintain local data into study management systems including setting up new studiesEnsure collection, review, track and provision of appropriate clinical documents to support regulatory submissionTrack and maintain adequate study related supplies in the office and facilitate their distribution to sites, including preparing and distributing Study File Binders and Site Initiation presentations/materialsProcess, reconcile, distribute and track essential documents and submit them to local archive in compliance with SOPsComplete tracking documentation as applicable including but not limited to spreadsheets, study and contract trackerPrepare and review site communication documentsSet-up/maintain courier accounts and organize shipmentsYou are:Experience as a CTA, within the pharmaceutical industry or CROExcellent organization skillsExcellent communication skills in English (Global environment)Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the businessStrong IT skills; experience with vTMF, mCTMS, and other Clinical Trials management systems preferredStrong communication with the ability to multitask and work effectively under pressureProfessional proficiency in EnglishWhat ICON can offer you: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. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work-life balance opportunities for you and your family
