Clinical Research Associate 2

As a CRA 2 you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The CRA is responsible for the initiation, monitoring and closure of assigned sites in clinical studies, in compliance with sponsor's procedural documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies. Primary point of contact between site staff and the sponsor. Acts as ambassador for the company and contributes to making the sponsor the preferred partner. Performing on-site monitoring visits according to plan, document actions and follow up on action plans. Site feasibility visits incl. analysis of site logistics, site personnel performance/quality indicators and accountability for patient recruitment strategies Train and guide site staff in the protocol and trial procedures to minimise protocol deviations (PDs) Train site staff in safety information handling and systems. ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.