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

Job Summary

This role involves comprehensive clinical trial monitoring and coordination within a full-service Contract Research Organization (CRO). The Clinical Research Associate (CRA) will be responsible for the planning, execution, and follow-up of monitoring visits (Site Selection, Initiation, Within-Study, and Close Out) and developing study-specific monitoring concepts and training plans for trial sites. A key aspect is coordinating communication between trial sites, sponsors, and project stakeholders to ensure smooth study progression. For large multicentric studies, the CRA will coordinate and provide technical guidance to a monitoring team (Lead Monitoring), ensuring uniform quality standards across all sites in compliance with CTR, ICH guidelines, and internal SOPs. The ideal candidate holds a natural science degree or medical/medico-technical training, possesses at least two years of relevant experience, and demonstrates excellent organizational and communication skills in both German and English.