- Monitoring of international clinical studies, preferably in the DACH region
- Site Monitoring: Act as the main contact in case of problems and questions regarding protocol and/or documentation
- Experienced handling ETMF and TMF
- Prepare/ assist the submission of study documentation
- Contact to internal and external stakeholders like pharmaceutical companies, health institutions and local authorities
- Assist with the periodic presentation about the status of the study to senior Management


- Education as nurse and/ or Bachelor/Master Degree in natural sciences
- 2-4 years of monitoring experience incl. supervision of clinical studies aligned to GCP regulations in place
- Experienced as a study nurse in a hospital setting, as a CRA at the CRO or at the sponsor
- Able to work independently as well as in a team
- Fluency in German, English and very good knowledge of French is a must. Italian language skills would be of advantage