Clinical Research Associate (CRA)

Eurofins • Harburg, Hamburg, Germany • Posted June 17, 2026

Location Harburg, Hamburg

Job Type Full-time

Category Life Scientists

Posted June 17, 2026

Job Description
The main task of the CRA is to act as a link between sponsor, CRO and trial site as well as to perform quality control of clinical trials. The focus is on clinical studies conducted in-house at bioskin or in the Northern German region.
Your main responsibilities: 
Perform all kind of the monitoring visits (site selection, initiation, periodic and close-out visits) as well as remote monitoring
Generation and updating of monitoring plans and site initiation presentation
Evaluating the quality and integrity of site practices
Act as contact for clinical trial suppliers and other vendors as assigned
Identifying and escalating protocol deviations, discrepancies in data, and non-compliance to clinical trial protocols
Close cooperation with the different departments in-house at bioskin as well as freelance CRAs
Compliance with protocol, GCP/ICH Guidelines
Qualifications
        

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