pAs Clinical Trial Administrator, you will keep clinical trials in Italy moving with accuracy and pace. Based in Rome, you will support the local study team from start-up to close-out – managing trial documentation, tracking progress, coordinating vendors and making sure investigator sites’ payments are on time. Your work keeps trials compliant and inspection-ready, so new treatments can progress towards the people living with serious chronic diseases who need them. /p h3What you’ll bring /h3 pYou pay close attention to detail, stay organised under pressure and like finding a practical way forward when issues come up. To succeed in this role, you will bring: /p ul liA Master’s degree in Life Sciences (preferably Biotechnology, Pharmacy, Chemistry, Biology or CTF) /li liA solid understanding of clinical trial phases, regulatory guidelines, Good Clinical Practice (GCP) and ethical considerations. /li liHands-on experience using Clinical Trial Management Systems (CTMS) and other digital tools to manage study documentation and track activities. /li liThe ability to manage multiple tasks, timelines and stakeholders and to keep milestones on track. /li liStrong written and verbal communication skills, and the ability to build good working relationships with internal and external stakeholders. /li liAnalytical and problem-solving skills to resolve study-related issues and suggest practical improvements. /li liIntegrity, sound judgement and a strong eye for detail. /li liOpenness to new digital tools and ways of working, and the flexibility to adapt in a fast-paced, changing trial environment. /li /ul h3Useful, but not essential: /h3 ul liExperience in the pharmaceutical industry or a Clinical Research Organisation (CRO). /li liCertification or formal training in Clinical Research and Good Clinical Practice (GCP). /li /ul h3What you’ll do /h3 pYou will provide administrative and operational support across every phase of the trials run by the local study team – preparation,



execution and close-out – making sure each study runs in line with regulatory requirements and the study protocol. As part of the Business Operations unit, you will also manage vendors and keep site payments running smoothly. /p pYou will: /p ul liSupport trial start-up by preparing and submitting the required documentation. /li liSet up and maintain the electronic Trial Master File (eTMF), including the Investigator Trial Master File (iTMF), so trial documentation is complete, accurate and compliant. /li liTrack trial activities and coordinate study tasks to support high-quality delivery and ongoing inspection readiness. /li liBuild and maintain relationships with internal and external stakeholders involved in vendor management. /li liMake clinical trial site payments on time, tracking and monitoring payments and resolving any issues quickly. /li liWork with colleagues across functions so that information moves smoothly and trial execution stays on schedule. /li /ul h3Who you’ll work with /h3 pYou will join the Clinical Development Centre (CDC), the dedicated hub for clinical operations in Italy, part of Research Development. Here, a team of passionate professionals brings Novo's global pipeline to Italian patients, running trials with excellence, agility and a shared commitment to quality. It is a place where curiosity is rewarded, collaboration is the norm, and every contribution has a direct impact on advancing therapies for people living with serious chronic diseases.br/ /p pReporting to the Senior Business Operations Manager,



you will collaborate closely with local study teams and colleagues across multiple functions, while also interacting with investigator sites and external vendors. Through effective management of trial documentation, tracking activities and investigator payments, you will help ensure studies run smoothly and compliantly, enabling teams to focus on delivering high-quality clinical research. /p h3What you can expect here /h3 pYou will gain hands-on experience across the full clinical trial lifecycle and across several therapy areas, building skills in trial operations, compliance, vendor management and finance processes. You will be trusted to own your work and make your voice heard, with the support of colleagues who value precision and collaboration. /p pAs part of a highly collaborative CDC team, you will be encouraged to continuously learn, take on new challenges and broaden your expertise. We are committed to developing our people, supporting them in achieving their professional goals, and fostering an environment where growth, continuous improvement and knowledge sharing are part of everyday work. /p pYou will also be encouraged to try new digital tools and ways of working, as we upskill our workforce in AI and technology. And you will be part of an organisation that has spent more than 100 years improving the lives of people living with serious chronic diseases. /p pFor this role, the Annual Base Salary ranges from 36,640.00 to 53,130.00 EUR, corresponding to the level of the position. The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge and relevant experience. /p h3Incentives and Benefits /h3 pThe salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks. /p pLearn more about our Reward Philosophy here . /p #J-18808-Ljbffr

📌 Clinical Trial Administrator (Italia)
🏢 Novo Nordisk A/S
📍 Italia