Description
Allucent is hiring a Clinical Research Associate (CRA) to independently monitor assigned clinical trials, manage site initiation, routine monitoring, close-out visits, regulatory affairs, site activation, and study-startup activities. The role requires at least five years of experience leading monitoring in complex trials, ideally in oncology or rare disease, strong ICH-GCP and regulatory knowledge, English and German communication skills, independent work capability, and willingness to travel throughout Germany, including eight days per month.
