Clinical Trial Administrator

16 ott - Roma
Experteer Italy

pIn 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. /pullishort-term incentives /lililong-term incentives /liliother employee benefits /lilisalary range 36,640 EUR to 53,130 EUR /lilireward philosophy /liliSupport trial start-up by preparing and submitting required documentation /liliSet up and maintain the electronic Trial Master File (eTMF) and Investigator Trial Master File (iTMF)



/liliTrack trial activities and coordinate tasks to support high-quality delivery and inspection readiness /liliBuild and maintain relationships with internal and external stakeholders involved in vendor management /liliEnsure site payments are made on time and resolve payment issues /liliCollaborate with colleagues across functions to keep trial execution on schedule /liliA Master's degree in Life Sciences /liliSolid understanding of clinical trial phases, regulatory guidelines, GCP, and ethical considerations /liliHands-on experience with Clinical Trial Management Systems (CTMS) and other digital tools /liliAbility to manage multiple tasks, timelines, and stakeholders /liliStrong written and verbal communication skills and stakeholder relationship-building /liliAnalytical and problem-solving skills /liliIntegrity, sound judgement, attention to detail /liliOpenness to new digital tools and fast-paced trial environments /li /ul #J-18808-Ljbffr

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