MAIN DUTIES Assist the Research team in the delivery of the NIHR research portfolio studies working within professional guidelines relating to the Code of Conduct, confidentiality, accountability and scope of professional practice. Delivery of high-quality evidence-based patient care under the direction of a Registered Nurse (or other registered professional as appropriate) with a focus on promoting health, self-care, and independence. With appropriate training, to take clinical samples for studies, and ensure the processing and storage and despatch of biological samples meets the requirements of the research protocol to make certain that safe handling and quality is assured. Undertake clinical procedures, venepuncture, standard observations. Acts as patient advocate. To support the safe administration of treatments and drugs given within the context of a clinical trial. Working without direct supervision (where appropriate) within designated parameters of the practice of the Nursing Associate role, specific research protocols and standards of operating procedures. Recognise issues relating to safeguarding vulnerable children and adults and report any problems or raise concerns to the appropriate registered care. Participate in the education and training of students of all disciplines. Use electronic records to record the outcome of assessment and evaluation of care. Assist in the assessment of and management of risk across the environment where care is being administered, recording and reporting any adverse events to senior members of the Research Team. Assist with the implementation and monitoring of clinical standards and outcomes. Develop a working knowledge of other providers resources and referral systems to ensure individuals needs are met, within the parameters of practice. Demonstrate a good understanding of principles of consent and ensure valid consent is obtained prior to undertaking nursing and care procedures. Demonstrate a good understanding of the Mental Capacity Act/Deprivation of Liberties and applies principles to everyday practice seeking advice/guidance from a Registered Nurse or another registered professional as required. Deliver effective care following plans determined by the registered nurse or other registered care professional and provide feedback on progress against the plan. Administration Accurately collect and record data ensuring it complies with the study protocol and regulations. Explain the study details to potential patients, including risks, benefits and procedures, ensuring they have clear understanding, reporting any concerns to the Senior Research Team members. Maintain accurate recruitment records on EDGE and specific study portals/protocols. Assist with promotion of studies using social media in line with BMG social media policy and NIHR/RDDN information governance Support in the identification and screening of potential eligible patients based on specific study criteria. Contributes and participates in audits, evaluation, and clinical standard setting within the Practice. Complete all required paperwork for legal and administrative purposes in accordance with relevant standards. Ensure that all practice policies are fully implemented. Work in accordance with all governance and internal systems relating to the management of clinical data and systems.