14 ott - Lazio
Experteer Italy
In this role, you will keep clinical trials in Italy moving with accuracy and pace, supporting the local study team from start-up to close-out.
You will manage trial documentation, track progress, coordinate vendors, and ensure investigator site payments are timely, maintaining compliance and inspection readiness.
You'll work within Novo's Clinical Development Centre to advance therapies for patients with serious chronic diseases, embracing digital tools and cross-functional collaboration.
You will be integral to delivering high-quality clinical research in a fast-paced environment.short-term incentiveslong-term incentivesother employee benefitssalary range 36,640 EUR to 53,130 EURreward philosophySupport trial start-up by preparing and submitting required documentationSet up and maintain the electronic Trial Master File (eTMF)
and Investigator Trial Master File (iTMF)Track trial activities and coordinate tasks to support high-quality delivery and inspection readinessBuild and maintain relationships with internal and external stakeholders involved in vendor managementEnsure site payments are made on time and resolve payment issuesCollaborate with colleagues across functions to keep trial execution on scheduleA Master's degree in Life SciencesSolid understanding of clinical trial phases, regulatory guidelines, GCP, and ethical considerationsHands-on experience with Clinical Trial Management Systems (CTMS) and other digital toolsAbility to manage multiple tasks, timelines, and stakeholdersStrong written and verbal communication skills and stakeholder relationship-buildingAnalytical and problem-solving skillsIntegrity, sound judgement, attention to detailOpenness to new digital tools and fast-paced trial environments#J-*****-Ljbffr
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