Clinical Research Associate

As a key member of the clinical operations team you will be at the forefront of clinical trials practice, implementing and monitoring trials, ensuring that sponsor and investigator obligations are met, and overseeing compliance with ICH GCP and FDA or European regulatory requirements. You will be working on a wide spectrum of projects in phase I-IV research at both GP practices and hospitals. In this role you can be operating out of offices in several German locations. Please plan a 2 weeks training period (if you consider applying for one of the other locations or for a home-based role)