About the job
- Preparation, execution, and coordination of clinical studies (Phases II – IV)
- Support and care for study patients
- Organization and coordination of diagnostics, laboratory work, and sample shipping
- Documentation of study data, primarily using electronic databases (eCRF)
- Preparation and facilitation of training sessions, monitoring visits, and regulatory inspections
- Communication with internal and external collaborating institutions
- Assistance with medical research projects
