As a leading company in Germany, we seek a Senior Clinical Research Associate to uphold quality standards for trial monitoring activities. The Sr CRA will conduct Selection, Initiation, Monitoring, and Closure Visits at Investigator Sites in line with project timelines. Compliance with project guidelines and Allucent SOPs is paramount for monitoring requirements. Ensuring adherence to GCP, ICH, and study protocols at clinical study sites is a key responsibility. Tracking study data collection and providing regular project status reports are essential tasks. Additionally, the Sr CRA will collect and review regulatory documents, prepare site visit reports, and document telephone contacts for comprehensive reporting. ‒ +
Homeoffice | Vollzeit | + weitere Benefits
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