Job Description
The following tasks and responsibilities are performed according to standard operating procedures within the CRU: - Prepare samples for processing (labelling and racking of collection/transfer tubes) and prepare study specific documentation prior to patient visits- Processing of biological samples (such as centrifugation, pipetting, biopsy fixation, preparing blood smears), storing and shipping of biological specimens to various analysis labs according to protocol requirements.- Co-ordinating courier collections for clinical trial samples. - Accessing data/information from Trust information systems as required.- Monitoring and maintaining sample laboratory kits and other consumables for use in CRU studies.- Performing routine laboratory duties such as preparing solutions, cleaning equipment, weekly stock checks and general housekeeping etc.- Data collection, and accurate completion of research documentation as appropriate, with meticulous attention to detail- Perform daily temperature monitoring checks using specialised temperature monitoring software (training provided)- Exercise independent judgement and initiative when problems arise by taking appropriate action to resolve the problem.- Liaising with visiting research teams for booking use of the laboratory for the processing and storage of trial samples.- To meet on a regular basis with the CRU Laboratory Manager for professional support and guidance- To attend training courses, conferences and study days in order to remain up to date with all relevant aspects of clinical research.- Deliver training in own discipline- To be aware of hazards within the laboratory and to comply with COSHH guidelines- To comply with ICH GCP
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