Job summary This is an exciting opportunity to join our successful Respiratory Research Team. The post holder will contribute actively to the conduct, coordination and delivery of research, under the leadership of the senior research nurse. Working effectively with the immediate and broader multidisciplinary team, being responsible for ensuring that high standards of clinical care planning, delivery, safety and patient satisfaction is to a very high standard, complaint with trust policy, study protocol requirements, local and national guidance and legislation. Main duties of the job The post holder will support the senior research nurse, principal investigators and associated multidisciplinary colleagues in the planning, scheduling, conduct, recruitment, patient care, support and data collection required for all studies within the department. They will be responsible for developing their own clinical practice, maintaining competencies (related to the research portfolio) and where appropriate taking delegated responsibility for the clinical elements of studies in line with trust policies and study protocols The post holder will be involved in ensuring that the research undertaken within the department safeguards the wellbeing of patients and is conducted within the confines of the ICH Good clinical practice guidelines for research EU directive, UK. The post holder will demonstrate a commitment to quality patient care through effective leadership and team working and will work at all times in accordance with the Nursing and Midwifery Code of professional Conduct and relevant professional guidelines. They will exhibit the Trusts Values and Behaviours and will model the way for others to demonstrate these in their practice. About us We are an acute trust caring for over half a million people in Wakefield and Kirklees. Our 10,000 staff work in patients homes, the community, and our three hospitals in Pontefract, Dewsbury, and Pinderfields (Wakefield). We prioritise our people and values so we can deliver the best possible care to patients. Our team is friendly, passionate, and innovative, always seeking better ways to work. We support work-life balance and foster a diverse, inclusive environment where everyone belongs. Our staff networks offer safe spaces to share ideas and concerns so we can increase awareness and appreciation of equality, diversity, and inclusion. We welcome applicants from all backgrounds and especially encourage members of the LGBTQ community, ethnic minority groups, and people with disabilities or neurodivergence to apply, as they are currently underrepresented in the Trust. If you value caring, high standards, improvement, and respect, join the MY team to make a difference every day. Application guidance: We understand that more applicants are using AI technology to help with their applications. While these tools can be useful, they cannot fully capture your skills, knowledge, and experience. Its important that you personalise your application. Relying solely on AI is not recommended, as it may reduce your chances of success. Our screening process is thorough, so if you have used AI, please make sure to disclose this on your application form. Date posted 03 April 2025 Pay scheme Agenda for change Band Band 6 Salary £37,338 to £44,962 a year Contract Permanent Working pattern Full-time, Flexible working Reference number C9377-CORP0967 Job locations Pinderfields Hospital Aberford Road Wakefield West Yorkshire WF1 4DG Job description Job responsibilities Develop a balanced portfolio of commercial and non-commercial studies Assess protocols and advise on safety, regulatory and logistical issues for the set up and running of the study/trial to ensure the well-being and safety of patients, participants and staff. To perform clinical trial coordinator duties (to include study setup, organisation and contribution to SIVs, project team meetings, delivery study visits) across a wide range of clinical trial areas. Planning the management of a specific research study, including the establishment and maintenance of office systems and adherence to project timescales and targets. Ensuring agreed recruitment metrics are achieved within the agreed timeline Identify barriers to participation in trials and develop strategies with clinicians, Trusts and others to overcome these barriers. Use appropriate computer software (EDGE) to process queries and provide reports on patient accrual. Participating in update meetings of the project team (both internal and external) to review the progress of specific projects. Publicising current trials to encourage new participants to join, and to maintain enthusiasm amongst existing participants by appropriate methods - mainly personal letters and the production of regular newsletters for specific projects. Ensuring that the data recorded on the case record forms (CRFs) of patients entered into specific trials or research projects are entered completely and accurately and within agreed timelines. Ensuring that any queries on the CRFs (missing or inconsistent or illegible data) for the specific trials or research projects are dealt with within agreed timelines. Provide participants with specialist information regarding their participation, including explaining all risk factors. Provide high standards and continuity of care for participants during the research study, maintaining lines of communication with clinical staff. Act as a resource to participants, their families and staff from within the clinical area, providing information and support; and to refer to other support agencies where necessary. Achieve and maintain defined competencies for clinical research to ensure that capability, skill and knowledge are appropriate to the work undertaken. Undertake, with appropriate training, interventional treatments directly to participants according to study/trial protocol and procedures and record the resulting information. Take and process clinical samples (e.g. venepuncture /cannulation)for studies, coordinate tissue sample collection and dispatch to relevant department or trial centre as appropriate. Maintain clinical skills as appropriate e.g. vital sign assessment, patient compliance, ECGs, flow rates and bladder scans. Attend relevant outpatient clinics to assist with recruitment, to monitor the progress and to collect data of participants involved in the study/trials. Attend inpatients involved in clinical trials as necessary to provide the care needed as prescribed in the protocol. Work at all times as part of the extended multidisciplinary team and maintain excellent links with the staff in clinic, ward and treatment areas regarding the protocol care required for study/clinical trial participants. Administer trial medications and treatments as appropriate. To recognise changes in patients conditions which require the intervention of others and refer on as appropriate? Support patients when receiving sensitive and life changing health information. To contribute to the development, implementation and delivery of training packages To deputise when required for the senior research nurse/AHP as required. This will involve working with staff at all levels and service users. The post will require high standards of integrity, confidentiality and attention to detail. Job description Job responsibilities Develop a balanced portfolio of commercial and non-commercial studies Assess protocols and advise on safety, regulatory and logistical issues for the set up and running of the study/trial to ensure the well-being and safety of patients, participants and staff. To perform clinical trial coordinator duties (to include study setup, organisation and contribution to SIVs, project team meetings, delivery study visits) across a wide range of clinical trial areas. Planning the management of a specific research study, including the establishment and maintenance of office systems and adherence to project timescales and targets. Ensuring agreed recruitment metrics are achieved within the agreed timeline Identify barriers to participation in trials and develop strategies with clinicians, Trusts and others to overcome these barriers. Use appropriate computer software (EDGE) to process queries and provide reports on patient accrual. Participating in update meetings of the project team (both internal and external) to review the progress of specific projects. Publicising current trials to encourage new participants to join, and to maintain enthusiasm amongst existing participants by appropriate methods - mainly personal letters and the production of regular newsletters for specific projects. Ensuring that the data recorded on the case record forms (CRFs) of patients entered into specific trials or research projects are entered completely and accurately and within agreed timelines. Ensuring that any queries on the CRFs (missing or inconsistent or illegible data) for the specific trials or research projects are dealt with within agreed timelines. Provide participants with specialist information regarding their participation, including explaining all risk factors. Provide high standards and continuity of care for participants during the research study, maintaining lines of communication with clinical staff. Act as a resource to participants, their families and staff from within the clinical area, providing information and support; and to refer to other support agencies where necessary. Achieve and maintain defined competencies for clinical research to ensure that capability, skill and knowledge are appropriate to the work undertaken. Undertake, with appropriate training, interventional treatments directly to participants according to study/trial protocol and procedures and record the resulting information. Take and process clinical samples (e.g. venepuncture /cannulation)for studies, coordinate tissue sample collection and dispatch to relevant department or trial centre as appropriate. Maintain clinical skills as appropriate e.g. vital sign assessment, patient compliance, ECGs, flow rates and bladder scans. Attend relevant outpatient clinics to assist with recruitment, to monitor the progress and to collect data of participants involved in the study/trials. Attend inpatients involved in clinical trials as necessary to provide the care needed as prescribed in the protocol. Work at all times as part of the extended multidisciplinary team and maintain excellent links with the staff in clinic, ward and treatment areas regarding the protocol care required for study/clinical trial participants. Administer trial medications and treatments as appropriate. To recognise changes in patients conditions which require the intervention of others and refer on as appropriate? Support patients when receiving sensitive and life changing health information. To contribute to the development, implementation and delivery of training packages To deputise when required for the senior research nurse/AHP as required. This will involve working with staff at all levels and service users. The post will require high standards of integrity, confidentiality and attention to detail. Person Specification Qualifications Essential Registered Nurse. Post registration qualification. Desirable Recognised teaching/assessing qualification. Research qualification (e.g. certificate/MSc in clinical research). Experience Essential Significant post registration experience. Experience of computer databases and administration. Working with a wide range of professionals. Experience dealing with highly complex situations. Experience providing and receiving highly complex information. Desirable Project management skills and experience. Data collection/analysis. Ability to critically analyse research findings. Clinical trial research experience. Understanding of research methodology. Experience of working in the respiratory environment. Person Specification Qualifications Essential Registered Nurse. Post registration qualification. Desirable Recognised teaching/assessing qualification. Research qualification (e.g. certificate/MSc in clinical research). Experience Essential Significant post registration experience. Experience of computer databases and administration. Working with a wide range of professionals. Experience dealing with highly complex situations. Experience providing and receiving highly complex information. Desirable Project management skills and experience. Data collection/analysis. Ability to critically analyse research findings. Clinical trial research experience. Understanding of research methodology. Experience of working in the respiratory environment. Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. Certificate of Sponsorship Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab). From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab). UK Registration Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window). Additional information Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. Certificate of Sponsorship Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab). From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab). UK Registration Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window). Employer details Employer name The Mid Yorkshire Teaching NHS Trust Address Pinderfields Hospital Aberford Road Wakefield West Yorkshire WF1 4DG Employer's website https://www.midyorks.nhs.uk/ (Opens in a new tab)