Clinical Research Associate Department: Clinical Development Centre If you are ready to help clinical trials in Spain deliver with quality and pace. A Master's degree in Life Sciences or a related field. Experience in clinical trial monitoring, or in a relevant role within the pharmaceutical industry or a CRO. Strong knowledge of ICH-GCP, clinical trial processes and applicable regulatory requirements. The ability to deliver high-quality, compliant trial execution, with a clear focus on patient safety and data integrity. Strong communication, planning and problem-solving skills, with the ability to build trusted relationships and take accountability for results. Protect patients and trial quality: perform monitoring according to study requirements, use data and risk insights to prioritise activities, and follow issues through to resolution. Improve how we work: use approved digital tools, share site insights and good practices,



and contribute to cross-trial initiatives in areas such as site engagement, quality and digitalisation, with opportunities to lead or co-lead according to your experience. Who you'll work with You will join CDC Spain and work closely with site teams, Trial Managers, Study Start-up, quality colleagues and other local and general partners to keep trials moving and sites inspection-ready. You will have clear expectations, support to develop your skills and opportunities to shape better ways of delivering clinical trials. Incentives and Benefits The 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.

📌 Clinical Research Associate (Madrid)
🏢 Novo Nordisk
📍 Madrid