Clinical Research Nurse/Allied Health Professional/Midwife

Dyddiad hysbysebu:	06 Ionawr 2026
Cyflog:	£38,682.00 i £46,580.00 bob blwyddyn
Gwybodaeth ychwanegol am y cyflog:	£38682.00 - £46580.00 a year
Oriau:	Llawn Amser
Dyddiad cau:	18 Ionawr 2026
Lleoliad:	Wigan, WN1 2NN
Cwmni:	NHS Jobs
Math o swydd:	Parhaol
Cyfeirnod swydd:	C9302-25-0606

Crynodeb

To be responsible for the management of clinical studies in accordance with the required standards, namely: Medicines for Human Use (Clinical Trials) Regulations; Human Tissue Act; UK General Data Protection Regulations (UK GDPR) and the Data Protection Act, other relevant laws, local Trust policies and procedures. To assist with programmes for recruitment, enrolment, screening and retention of research participants in accordance with the UK Policy for Health and Social care Research; ICH Good Clinical Practice (ICH GCP) guidelines and protocols. Duties: To attend MDT meetings, and appropriate clinics, to promote NIHR RRDN study participation and to screen and recruit new participants, and to act as a resource to the members of the MDT. To work with the network Clinical Trials Co-ordinator to facilitate the speedy set up and approval of NIHR RRDN studies. Complete extensive feasibility assessments of all studies ensuring the Trust has both the capacity and capability to run the research study. To ensure all necessary approvals and other agreements are in place prior to commencing the study. To ensure all members of the site team are GCP trained with current CV and any relevant study training is completed. The delegation log must be complete and signed with duties assigned by the PI prior to commencement of study To ensure that study specific investigations are undertaken as required by the study protocol, in order to establish eligibility and safety to enter the study. To help the investigator facilitate the informed consent of a participant (appropriate to age and understanding) and maintain PI oversight is maintained throughout the study. To ensure the safe administration of treatments and drugs given within the context of a clinical study. To ensure blood and other samples are collected as required by the protocol. To maintain accurate documentation of clinical events. To accurately document data collected into the case report forms (CRF). To be responsible for forwarding study data in a timely manner to the sponsor. To monitor treatment toxicity/side-effects. To record and report all adverse events as they occur as part of a clinical trial in accordance with the protocol and delegated responsibilities. To maintain accurate and legible patient notes (written and electronic) in accordance with Trust and national professional policies and guidelines. To work with the investigator and ensure that clinical trials are appropriately archived. To act as a primary contact point (for study issues) for the patient for the duration of the study. To provide support to the local investigator as required. To work with local services, the multidisciplinary team and the regional network to develop strategies to overcome barriers to recruitment. To supply data as required to the RRDN Research Lead regarding progress of network studies. To keep local and network staff informed of the progress of RRDN studies. To provide highly specialised research advice to patients concerning the care and treatment during participation in research. To provide information in a way that is suitable for the patient, including the manner in which the information is disseminated, complexity and language used and the timing of its giving. To provide education and support to patients regarding clinical studies. To communicate effectively with local staff and the network team. To ensure all communication is evidenced and documented as required by governance standards. To maintain confidentiality at all times and work within the Data Protection Act with all research activities. Planning and Organisational Duties The post holder will participate in and influence care delivery by: working with network staff to develop knowledge and understanding relating to the conduct of clinical research studies in the NHS. attending relevant training (e.g. Good Clinical Practice) to ensure all research is conducted correctly. maintaining evidence of competency in the area of research. acting as a resource and provide expertise to other local staff involved with RRDN studies at the site. continuing professional development, keeping updated with current clinical practice to maintain professional registration and ensure practice is within Research SOPs and Trust guidelines and policies. attending meetings in relation to clinical research as required. providing assistance and support to other research staff within the Trust as required. Communications and Key Working Relationships Act as a point of contact for trial sponsors and monitors and communicate directly with them regarding data queries, AEs, SAEs and other enquiries relevant to the trial and research team. Communicate with the PI and relevant ward/outpatient managers to facilitate patient visits. Liaise with staff at all levels, both internal and external relating to trial activities, regarding information whilst maintaining confidentiality at all times. Attend MDT meetings Liaise with radiology and pharmacy departments within the hospital regarding the capability and capacity to run new research studies. Be the first point of contact for the research participants, deal with patient queries in a professional caring manner and refer to medical team when required. Raise research study awareness within the speciality, involving ward staff and other members of the multidisciplinary team to ensure patients are aware of the research studies available to them. Promote research awareness throughout the Trust. Responsibility for Finance Ensure that office and clinical supplies are adequate, ordered and obtained for the smooth running of the research studies. Liaise with the clinical trials assistant for reordering supplies in a timely manner. Liaise with Sponsors for supply and resupply of blood kits and specific equipment for studies. Ensure all research studies are costed correctly and work closely with R&D to ensure all costings for the trial are included at set up. Ensure the patient visit tracker is updated following patient visits to aid invoicing. Responsibility for Human Resources Adhere to Trust policies and maintenance of the professional Code of Conduct. Provide training and mentorship to clinical trial administrators. Provide mentorship to new research nurses in post. Expected to follow all relevant protocols, SOPs and standard practice. Plan and organise own time and workload activity effectively. Able to work independently using own initiative or as a team when required. Consult with Senior Research Nurse Manager as point of reference for any queries and will meet regularly with staff. Consult with Head of Research for further guidance if required. Responsibility for Health & Safety Compliance with the Health & Safety at Work Act 1974 the post holder is required to fulfil a proactive role towards the management of risk in all of their actions. This entails the risk assessment of all situations, the taking of appropriate actions and reporting of all incidents, near misses and hazards, and a statutory duty of care for their own personal safety and that of others who may be affected by their acts or omissions. Responsibility for Teaching The post holder will promote life-long learning through the use of appropriate coaching, teaching and assessment in practice by: Having the opportunity to mentor staff new to research and be responsible for introducing student nurses to research on day placements. Work Circumstances & on-call This post is normally Monday to Friday, however there may be times when you will be asked to work outside these hours.