Clinical Research Associate (CRA) / Clinical Monitor | Biologe (m/w/d)

Job Summary

This role is for an experienced Clinical Research Associate (CRA) or Clinical Monitor, responsible for ensuring the smooth execution of clinical trials (Phases I-III) across multiple sites, primarily within Germany. Key responsibilities include planning, executing, and following up on all monitoring visits (Site Selection, Initiation, Study, and Close Out), developing study-specific monitoring concepts, and training plans for investigative sites. The CRA will also coordinate communication among sites, sponsors, and project stakeholders. A significant component involves leading and providing technical guidance to a monitoring team (Lead Monitoring) on large multicenter studies, ensuring adherence to CTR, ICH guidelines, and internal SOPs. The ideal candidate must possess a scientific or medical background, at least two years of relevant experience, and excellent communication skills in both German and English, coupled with a willingness to travel.