Cardiac Research Practitioner (CRP)/ Cardiac Research Nurse

Dyddiad hysbysebu:	18 Gorffennaf 2025
Cyflog:	£42,939.00 i £50,697.00 bob blwyddyn
Gwybodaeth ychwanegol am y cyflog:	£42939.00 - £50697.00 a year
Oriau:	Llawn Amser
Dyddiad cau:	31 Gorffennaf 2025
Lleoliad:	Harrow, HA1 3UJ
Cwmni:	NHS Jobs
Math o swydd:	Parhaol
Cyfeirnod swydd:	C9337-25-2761

Crynodeb

KEY RESPONSIBILITIES Key Working Relationships The multi-disciplinary cardiac research team Investigators Clinical staff Trust Research & Innovation Department Study sponsors Study vendors NIHR RRDN North London Clinical Trials Pharmacy Team Research and Clinical To facilitate safe, efficient, patient focussed research. To demonstrate sound knowledge of the life cycle of a research project from inception to study close out and perform all clinical protocol related tasks independently as a lead study coordinator to include: Ensuring all site staff are trained, delegated and appropriate approvals are in place for studies. Patients are pre-screened, approached and recruited in a suitable way, having a detailed understanding of the informed consent process and clinical patient pathway. Planning of the schedule of events and study visits is taken to ensure the study is delivered safely and to protocol. Safely and accurately perform, record and capture administrative and clinical assessments in medical notes. Collect, store and transfer biological samples in accordance with study protocol, trust policies and safe shipping legal requirements. In an accurate and timely manner transfer source data to electronic case report forms (eCRFs) and respond to data queries. Monitoring of the patient within the study visit: be able to recognise and respond appropriately to deteriorating/ urgent/ emergency situations. Recoding and reporting of adverse events. Ensuring Investigation Medicinal Product procedures are performed according to staffs competency and scope of practice and to both Trust and Sponsor protocols. Maintaining the Investigator Site File and departmental shared drive to the highest standards. Maintain a suitable and in-date supply of study supplies e.g. as lab kits, needles. Providing Sponsors and Investigators with data and information as required and responding positively to requests. Coordinate and facilitate productive Sponsor, regulatory and R&D monitoring visits and responding to action items in a timely manner. To work according to ICH-GCP and research governance standards for clinical research studies. To be competent in a range of clinical skills required for research studies and be willing to undertake training for new skills. To be competent in a range of IT and administrative skills required for clinical research and be willing to undertake training for new skills. To be fully trained and competent in all aspects of study medication storage, transport and administration (within scope of practice, depending on type of professional registration): adhering to all requirements of the Clinical Trials Pharmacy Team. To ensure accurate and comprehensive medical and research records are maintained using appropriate documentation. To recognise and act on concerns raised if research deviates from the study protocol or the study design conflicts with legal or patient safety requirements. To identify barriers to recruitment and implement agreed action plans as required. To manage own caseload of clinical research studies, working collaboratively with wider multidisciplinary teams. Provide supervision, training, and support for junior colleagues, especially in the conduct of CTIMP clinical trials. To be trained and delegated on all departmental research studies to provide cover for any staff absence. To provide thorough verbal and written handover of own workload prior to any planned leave. Attend meetings relevant to the clinical and research area and disseminate information to colleagues. To act as a knowledgeable resource in clinical practice and research, promoting an active and effective research culture. To ensure all departmental equipment is calibrated and maintained according to study and Trust requirements and calibration certificates are appropriate shared with Sponsors. To respond to patients and carers/family members in a timely, respectful and considerate manner. Act as advocate for patients to enable them to make informed decisions regarding study participation. There may be barriers to understanding complex clinical trials. Exercise a high level of personal and professional autonomy and critical judgement when assessing patients in clinical follow up visits and when giving advice to patients on the telephone. Deliver health education within research visits and provide advice to patient, family and other members of the team. To liaise and communicate effectively any changes to patient care with other members of the clinical team and outside agencies as required. To liaise with Ward Pharmacists, Clinical Teams and Clinical Trials Pharmacy when clinical trial patients are hospitalised to ensure patient safety as prescribed drugs for hospitalisations may interact with clinical trial medication. Responsible for accurately entering details of patients and their treatment into clinical computer based and paper-based systems. Communicate with research team and/or research admin staff to ensure timely ordering of necessary stocks. Administration To work at all times in a methodical manner, with a high attention to detail. To manage running of own allocated clinical research studies on a day to day basis, which requires coordination with the wider team, other healthcare professionals in the multi-disciplinary team and outside agencies. To be an expert for assigned clinical trials and to ensure the promotion and delivery of high standards of clinical care and clinical practice. Able to prioritize workload, delegate where appropriate and alert manager when help is required. Able to plan own workload in accordance with trial specific protocol and schedule of assessments. To promote effective working relationships between all members of staff to develop professionalism throughout the department. To be able to problem-solve communication barriers and act appropriately. Adhere to Trust policies pertaining to patient confidentiality/ GDPR /Caldicott Recommendations. Reimbursing patient travel expenses, providing patient refreshments and booking patient taxis. Education and Training To act in accordance with the NMC Code of Professional Conduct for Nurses, Midwives and Health Visitors and to be always accountable for own clinical practice and professional actions (Nurses only). To ensure continued registration with the NMC (Nurses only). To act in accordance with the NIHR/AHCS Standards of Proficiency for CRPs and Scope of Practice for CRPs (CRPs only) To be accredited or working towards accreditation on the AHCS Accredited Register for CRPs and to maintain continued registration (CRPs only) To participate in departmental reflection sessions between CRPs and Research Nurses as part of ongoing professional revalidation processes and to support ongoing learning and personal insight. To deputise for the Senior Cardiac Research Practitioner/Nurse as required. To develop and maintain knowledge of cardiovascular conditions, treatments, and investigations. To ensure ongoing compliance with mandatory training. To maintain regular Good Clinical Practice training as required. To undertake clinical and research competencies as required. To undertake annual trust appraisal process to support personal and professional development. To support and supervise in the induction, training and ongoing development of junior staff, newly recruited staff and work experience students in the department. To support in the training and education of other healthcare professionals working on research studies. To identify and attend relevant external and local training which contributes to ongoing personal and professional development. To attend study training, investigator meetings and conferences as required. Participate significantly towards research department improvement projects, setting standards, audits and monitoring quality within the area of clinical research. Department Specific Requirements To prioritise patient safety at all times. To treat all research patients and their families/carers with the greatest respect and consideration, going above and beyond to ensure they have a positive experience of participating in clinical research, supporting retention in all research studies. To work flexibly outside of usual hours where required to meet patient, study or department needs. Willingness to deliver research studies in areas outside of the immediate department e.g. A&E. To contribute to the development of departmental policies and SOPs, adhering to these and those of the Trust at all times. To ensure that the Cardiac Research Department complies with ethical, regulatory, legal, Trust and R&D standards at all times. To attend investigator meetings, which may be international, when required. General Frequent and prolonged sitting at computer terminal. Travel long distances to departments and wards with which face-to-face liaison occurs (such as A&E and R &D) which are not in close proximity to the department.