Clinical Research Associate

  • Sector:


  • Contact:

    Kasia Krasuska

  • Contact email:

Clinical Research Associate 

Our Munich based client, specialising in manufacturing life-saving medical devices is currently looking for a CRA to support clinical project management through the duration of the study.


Some of the responsibilities will include:

  • Providing support in developing and writing clinical study documentation, while ensuring its compliant with the clinical study protocol as well as ISO 14155

  • Participating in co-monitoring visits as and when required at clinical sites in France, Germany & Belgium (once every other month)

  • Submission of study specific documents to regulatory authorities

  • Collating, filing and general administration of study documentation

Experience required:

  • Successfully completed technical or scientific studies or comparable qualification

  • Experience in working with medical device is essential

  • Working knowledge of the legal requirements for either medical devices or pharma, such as: ICH-GCP, ISO 14155

  • Excellent oral and written communication skills

  • Fluency in both German and English languages

Please apply with your CV or contact Kasia Krasuska for further details on this opportunity and additional vacancies in Regulatory Affairs and Quality Management.

+49 30 16 63 83 76


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