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: 

  • 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

    The ideal Candidate will need the following experience to be considered:

  • Min. 2 years of the clinical monitoring experience (preferred Dermatology)
  • Degree in a scientific or medical discipline or equivalent
  • Very good knowledge of Good Clinical Practice/ICH Guidelines
  • Proven ability to work independently in a fast-paced environment
  • Excellent communication, interpersonal, and organizational skills
  • Fluency in German and a high level of English language
  • located in Hamburg

    • Additional Information

    Contacts by headhunters, recruiting or staffing agencies are not accepted!

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