The role of the Clinical Research Associate (CRA) is the primary point of contact between investigational site and Novo Nordisk. You will be responsible for taking leadership of site management for the selection and initiation of sites as well as conduction and closing activities of the appointed studies in compliance with local regulations, ICH-GCP, company procedures and protocol requirements to ensure date quality and study subject protection. You will be responsible for recruitment at country/ site level and thereby delivers results that have a direct impact on the successful completion of the clinical programme. You coordinate with the Project Manager and communicates to them progress and critical issues that may impair trial success. You will be responsible for the recruitment at site level and communicate to the local trial manager for any progress and/or issues that may in pair trial progress.