Dr. Ruth Geraldes (lead of the MS clinical trials group) and Dr Isabel Leite (Consultant Neurologist) are seeking a part time Research Nurse to support clinical research in the field of neurological conditions and neurodegeneration, in line with the aims of the NIHR UK Clinical Research Network (UK CRN). Based at the John Radcliffe Hospital, the post-holder will assist in the provision of a clinical study service. You will be responsible for managing the care pathways for patients and carers participating in clinical studies focused on Neurological conditions (e.g. MG, MS, NMO) This will involve the recruitment and monitoring of study patients and the collection and documentation of accurate data including collection and management of tissue and/or blood samples. You will work collaboratively with the vibrant and enthusiastic clinical studies teams and the wider multi-disciplinary teams in the management of your own caseload of clinical study patients. The role involves using an in depth knowledge of trial protocols and their application in practice, alongside a working knowledge and compliance with the local, national and international research regulations. This post would suit someone with a clinical background in Nursing, with a desire to engage with hands-on clinical trials/research.

Main duties of the job

Employed as a staff nurse to facilitate the research pathway for participants in clinical trials. Will be directly involved in:

o assessing, planning & implementing care for clinical trial participants during research visits.

o collection and documentation of accurate data and record of care if appropriate.

o provide support for a range of research studies and be expected to be flexible to work across a broad portfolio.

o assist in the recruitment & retention of participants. Fulfil the expectations and capabilities as delegated by the Sponsor, Chief Investigator or Principal Investigator as set out in GCP & Research Governance Framework Work collaboratively with OUH service delivery colleagues to ensure high quality participant care and experience. You will be responsible for assessing and managing the care pathways for patients and carers participating in clinical studies focused on Neurology. You will work collaboratively with the clinical trials team and the wider multi-disciplinary team in the management of your own caseload of clinical trial patients.

About us

The National Institute for Health Research (NIHR) is funded through the Department of Health to improve the health and wealth of the nation through research. The CRN: Thames Valley and South Midlands is one of 15 local Clinical Research Networks in the NIHR Clinical Research Network (NIHR CRN). The NIHR CRN is the clinical research delivery arm of the NHS in England, tasked with supporting the rapid setup and effective conduct of studies, so that researchers can gather the robust evidence needed to improve treatments for NHS patients. These local Networks drive clinical research delivery performance across the locality, and champion the role of clinical research in the NHS at every level. The CRN: Thames Valley and South Midlands is hosted by Oxford University Hospitals NHS Foundation Trust and works in partnership with local NHS Trusts to fulfil the aims of the NIHR CRN. The CRN: Thames Valley and South Midlands supports clinical research in Oxfordshire, Buckinghamshire, Berkshire and Milton Keynes.

Job description

Job responsibilities

3 Key Areas of Responsibility3.1 Clinical Plan and coordinate your day-to-day work in collaboration with the Senior ResearchNurse management team. Ensure the safe administration of treatments given within the context of a clinical trial. Manage a caseload of people who have consented to participate in certain studies. Undertake study procedures required and in line with the research protocol. Provide accurate and timely information, education and support to patients (and theirsignificant others) regarding clinical research. Maintain accurate documentation. Have an understanding of adverse event reporting and recording, and ensure that thePrincipal Investigator and Central Study Team is made aware of any such events. Act at all times in a way that maintains patients and carers dignity. Refer to other specialists as required in order to provide optimal patient care.3.2 Research Work according to GCP and research governance standards for all aspects of workpractice. Support studies running in both the community and in the clinical trial units Act as Study Co-ordinator for Clinical Trials and Research Studies, under indirectsupervision of Senior Research Nurse Input to recruitment strategies. Support and assist in the development of action plans asrequired Assist in the identification of patients eligible to enter clinical studies. Have an awareness of legislation and the Mental Capacity Act take informed consent asper study protocols. Register/randomise patients into studies. Adhere to clinical study protocols and report protocol deviations and violations to studycoordinator. Ensure that clinical trial records are accurately maintained. Ensure that own case report forms are accurately completed, in paper and electronicformat. Communicate effectively with the rest of the study team and patients/carers. Support the Senior Research Nurses in the event of inspection from a regulatory and/ormonitoring authority. Provide support for clinical trial colleagues in their absence. Attend meetings relevant to the nature of the job. Keep up to date with departmental, Trust, NHS, and EU developments for themanagement of clinical research Travel as required by the network to research locations across the organisation.3.3 Administration Use computer network and the internet. Ensure that all data is handled according to the Data Protection Act and in a confidentialand where necessary anonymised fashion.3.4 Education and Training Promote research within the Trust and across the network in relation to clinical trials. Assist in the education and support of clinicians and service users. Continue your own personal and professional development keeping updated with currentpractice. Contribute to performance development review processes Proactively seek opportunities for personal development and progression. Attend national meetings and training as relevant to role.4 Other Understand and adhere to Trust policies and procedures, including trust mandatory andstatutory training. Act in accordance with the NMC Code of Professional Conduct or equivalent. Ensure that trust wide standards are maintained and monitored to improve the quality ofcare to all those who come in contact with the service provided by Oxfordshire andBuckinghamshire Mental Health Partnership NHS Trust. The post holder hasresponsibility for safety as outlined in the hospitals policy and Health and Safety WorkAct 1974. Maintain patient confidentiality at all times. This job description is an outline only and does not contain an exhaustive list of dutiesand you may be required to undertake additional responsibilities. It may be amended bythe Consultant Neurologist following discussion with the post holder.

Person Specification

Education

Essential

• Level 1 registered nurse or equivalent professional qualification

Desirable

• n ? Evidence of post-registration learning and development ? Postgraduate training ? Dual qualified (RGN and RMN)

Employer details

Employer name

Oxford University Hospitals NHS Foundation Trust

Address

John Radcliffe Hospital

Headley Way

Oxford

OX3 9DU

Any attachments will be accessible after you click to apply.

321-CORP-6073928-B6-1