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Clinical Research Associate (CRA)

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Eurofins
πŸ“ Harburg, Germany
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Location Harburg
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Posted June 09, 2026
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Commute Local Area
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Job Description

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:Β 

  • 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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    πŸ“ Location Details

    πŸŒ†
    City
    Harburg
    πŸ—ΊοΈ
    Country
    Germany
    πŸš—
    Commute
    Local Area

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