Nurse

Collection of bio samples for screening process and during the study. Perform ECG of the volunteer/subject during screening and if applicable, for study. Recording vitals of the volunteer/ subjects. Preparation and labeling the vacutainers and RIA vials. Cannulation and removal of cannula for the blood sampling during the study as required by the protocol. Observation of subjects for adverse events and reporting the same to the duty doctor/investigator immediately. Coordinating with the Investigator/duty doctor in the management of adverse event. Performance of blood glucose testing by Glucometer as per protocol requirement. Handling of bio samples [as applicable] includes collection, receipt, centrifugation, separation storage and shipment. Managing Bio waste for their disposal. Collection of urine and blood samples for screening and safety analysis To carry out any other responsibility as and when assigned by the Head-Human Pharmacology Unit / Head of Syngene Clinical Development Team.