Specialised in
- Register trials
- Clinical trials
- Consultation for ethical aspects
- Support for submitting protocols with CTC/EC
- Explain trial to patient and take ICF (together with PI)
- Plan examinations and appointments
- Prepare and (help) perform trial visits
- Process samples (both blood and urine) and send by mail
- ECG
- Data entry and management (both source and eCRF)
- Prepare and guide monitoring visits