The Contract Research Nurse provides shall be responsible for the below activities:

• Visit patients’ home for performing clinical trial assessments as prescribed in the clinical study Protocol.

• Perform all assessments and procedures in accordance to the ICH GCP guidelines and local regulations.

• Monitoring of vital signs during home care

• Monitoring of blood glucose levels

• Complete evaluation tasks, including identifying changes in medication and vital signs.

• Administer Investigational Products to the patient according to the study protocol.

• Collect blood / biological samples as per the study protocol.

• Perform processing of blood samples using Centrifuge.

• Ability to complete the study documentation like QoL Questionnaires, Patient Diaries etc.

• Coordinate with PI and Clinical Trial Site team for the study related documentation / materials handover.

• Coordinate with the research team for shipment of samples.

• Keep the patient comfortable while performing the assessments.

Art der Stelle: Werkvertrag