1. Adhere to standard operating procedures without direct supervision. 2. Assist Clinical Trial Delivery Team in the delivery of UHPNT Research Portfolio. 3. Demonstrate responsibility for own actions and awareness of own limitations. 4. Using initiative daily in order to plan and effectively maintain individual diary and workload. 5. Attention to detail and accurate record keeping of all patient visits. 6. Flexible approach to work and can remain calm and professional in a busy environment. 7. Clinical procedures of the role, venepuncture and cannulation, history taking, standard observations (height & weight, BP, RR, HR, Oxygen saturations, temp) disease specific outcome measures, questionnaires, rated scales as required. Ensure that the results are interpreted and if required discussed with wider clinical team as needed. 8. Support data collection that will assist the R&D department in high standards of GCP (Good Clinical Practice). 9. Sample processing of clinical trial samples ensuring safe use of centrifuge and following procedures as defined by the trust. 10. Data accuracy and IT skills are essential to this role and combining clinical skills with these demands can be mentally difficult. Undertaking data entry is a requirement for this role and can often require long periods of concentration. For further details please see the attached JD &PS