Clinical Research Associate II (all genders)

You will be responsible for a selection of studies – from the selection of centers to implementation and completion. You will work closely with local CRA colleagues in various study teams and contribute to the timely project completion through proactive planning. You will supervise a selection of test centers and monitor cooperation with partners and authorities. You will ensure that all internal and external regulations are observed in your projects and that the test centers are ready for inspection at all times. The candidate should have planning skills, excellent organizational skills and analytical thinking skills, independent and structured way of working, excellent social skills.