Department: Clinical Development Centre Spain As a Clinical Research Associate in CDC Spain, you will be a trusted partner for your clinical trial sites, helping studies deliver with quality, pace and a clear focus on patients. Our CRA vision combines strong site partnerships, smarter ways of working and risk-based quality management. 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. 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. You will join CDC Spain and work closely with site teams, Trial Managers, Study Start-up, quality colleagues and other local and integral 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. 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. Learn more about our Reward Philosophy her e .

📌 Clinical Research Associate (España)
🏢 Novo
📍 España