Description
We are seeking a Clinical Research Coordinator to support a clinical study at a testing centre in Munich. The role involves working 20 hours a week for 52 weeks.
As a Clinical Research Coordinator, you will assist the study team with the conduct of the clinical study. Your tasks may include:
- Supporting the organisation and coordination of the study workflow
- Caring for study patients during scheduled study visits
- Preparing and coordinating patient visits
- Assisting with study-related documentation and data collection
- Maintaining and updating study documentation
- Collaborating with investigators and other members of the study team
- Supporting administrative and organisational tasks related to the clinical study
- Ensuring a structured and smooth study workflow at the testing centre
Requirements:
- Completed training in a medical or nursing field, e.g. as a healthcare nurse, medical assistant or comparable qualification
- Experience as a Clinical Research Coordinator, Study Nurse or study coordinator
- Experience in a clinical trial environment
- Good organisational skills and careful, structured work
- Secure handling of medical documentation
- Excellent communication and teamwork skills
- Good German language skills
Benefits:
- Location: Munich
- Working hours: 20 hours per week
- Duration: 52 weeks
- On-site deployment at a testing centre in Munich