Clinical Research Nurse

Work autonomously and assist in the management of a caseload of clinical trial patients whilst working as part of the MDT. Maintain effective communication with patients, carers and professionals to ensure high quality service delivery Identify suitable patients for entry into clinical trials by attending clinics (screening notes) and relevant MDT meetings Maintain accurate documentation of patient events in the medical notes Ensure trial consent protocols are adhered to Demonstrate a comprehensive understanding of treatment options, treatment side effects and disease processes to support informed treatment choice for patients Provide ongoing information, education and support to patients (and their significant others) and all levels of staff regarding clinical trials and specific trial treatments Take and assist in the consent of patients and randomisation of patients to treatment arms Ensure that trial specific investigations are undertaken as required by the trial protocol and obtain
results in order to establish eligibility and safety to enter the trial Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial Monitor treatment toxicity/side effects and initiate changes to treatment or treatment cessation as required by trial protocols Report and record adverse events which occur whilst patients are under trial therapy to the trial co-ordinator/Principal Investigator and relevant local and regulatory authorities Provide continuity of care to patients and their carers throughout the trial programme. Provide specific advice and psychological support as appropriate. Refer to other specialists as required to ensure optimum patient care. Act as a primary contact point for the trial participant Maintain accurate patient trial documentation, complete Case Report Forms, including the use of electronic data capture systems and ensure relevant information is recorded in patients medical notes. Perform phlebotomy, blood and
urine spinning as required by trial protocols, ensure the safe handling, storage and transportation of samples