项目介绍

2026年9月8日

Your responsibilities

• You will coordinate and manage all aspects of your own clinical research project and support others.
• As part of this role, you will recruit study participants in accordance with the study protocols.
• Research data will be collected, managed, and entered into study databases by you with accuracy and attention to detail.
• You will analyse research data and contribute to the interpretation of study findings.
• Your research findings will be presented at international scientific conferences.
• You will publish research results in peer-reviewed scientific journals.
• Throughout their thesis projects, you will support and supervise Master’s students.

Your profile

• Master in Medicine, Biology or Psychology
• Knowledge of the Good Clinical Practice (GCP) Guidelines E6(R3) and Swiss regulatory requirements would be an advantage.
• Excellent oral and written knowdlege in German and English
• Interest in working in a clinical study team, with patients – especially children and their parents
• Attention to detail
• Structured process thinking
• Ability to cope with frustration
• Ability to work independently but also as a part of the team

Information on your application

Please apply through the Zurich Chidlren’s Hospital Jobportal