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

Job Summary

This role is for an experienced Clinical Research Associate (CRA) or Clinical Monitor, responsible for the planning, execution, and follow-up of monitoring visits (Site Selection, Initiation, Within-Study, and Close Out) for clinical trials across phases I-III. The successful candidate will develop study-specific monitoring concepts and training plans for trial sites, ensuring smooth study progression by coordinating communication among sites, sponsors, and project stakeholders. A key aspect involves coordinating and providing technical guidance to a monitoring team (Lead Monitoring) to ensure consistent quality standards across multi-center studies, strictly adhering to CTR, ICH guidelines, and internal SOPs. The position requires a natural science degree or medical/medical-technical qualification, coupled with at least two years of relevant experience. Excellent organizational, communication (German and English), and proactive skills are essential, along with a willingness to travel within Germany.