Job description Visit patients home for performing clinical trial assessments as prescribed in the clinical study Protocol Perform all assessments and procedures in accordance with the ICH GCP guidelines and local regulations Monitoring of vital signs during home care blood pressure heart rate recording of ECG temperature and oximeter statistics 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 Discard the generated Bio-Medical Waste during the visit by handing over to appropriate biowaste disposal agency Confirm with the research team to discard the Bio Medical Waste at site or near local facilities Complete the study documentation like Source Documents 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 Coordinate and support scheduling patient visits patient follow-ups and completion of protocol required assessments by investigators Escalate potential issues to Regional Project Coordinator Central Project Coordinator and site team representative Job Types Contractual Temporary Freelance Contract length 12 months Pay 1 000 00 - 1 300 00 per day Work Location Remote