Total 1,010 job vacancies by NHS Jobs

Please see attached Job description and person specification for full details of roles and responsibilities.

Please see attached to the advert a job description and person specification for further details. Please ensure you read both documents carefully. Please note, if your application is successful you will be required to present original certificates of qualifications that are listed in the person specification under essential.

To record electrocardiograms and produce a report To perform spirometry and produce a report To perform and measure automatic and manual blood pressure measurements To obtain venous blood samples when needed To set up and fit a cardiac monitor, 24-hour ambulatory ECG monitor, and a 24hr ambulatory blood pressure monitor To prepare equipment and clinical areas for Cardiology investigations Receive and assist patients and/or carers to prepare for Cardiology investigations Obtain additional information that will assist with planning and preparing of Cardiology investigations Support patients and/or carers during investigative Cardiology procedures To take an active role in the resuscitation of patients (Basic Life Support) To give support advise to patients and/or carers/medical team following completion of investigative Cardiology procedures To organise the patient journey and assist in the Cardiology clinics if required To chaperone Cardiology medical staff in the above Follow manufacturers/protocol instructions and operate equipment Assess and maintain equipment and devices for safe use during Cardio-respiratory investigations Report faulty equipment to the Team Leader Communicate technical equipment-related information to healthcare colleagues, patients, carers, and suppliers Use safe manual handling techniques when moving both patients and equipment Contacts medical/nursing staff to advise of adverse/life-threatening test results Follow departmental and national policies and procedures to maintain safe practice To undertake clerical duties as required including sending out appointments using the trust systems, filing, photocopying, and handling incoming and outgoing post To organise and prepare patients information, ready for investigation collect notes and identify as correct on equipment as necessary Records personally generated information and update records. Also to learn how to input results of investigations performed by other members of staff To attend to general tidiness of department including unpacking and storage of ward stock deliveries Assist with maintaining stock levels and supplies. To answer the telephone and relay messages appropriately To undertake department errands as required Assist in the safe use, custody and maintenance of equipment, utilising resources effectively and efficiently. When required to, act flexibly within the role which may include moving to other sites within the trust and/or change to duties in consultation with your line manager.

Adhering to GCP at all times. Responsible to support existing team and support current portfolio and develop it further and work to recruit to time to target. Working closely with Research Manager, R&D Lead, Chief Investigators, Principle Investigators, Local R&D, REC, external stakeholders. CLINICAL: Work autonomously to manage and coordinate existing and new portfolio of clinical research whilst working as part of a multidisciplinary team. Maintaining effective communication with patients, carers and professionals to ensure service delivery. Assist in selecting, screening and organising the patients and/or volunteers suitable for entry into clinical trials/studies when applicable. Ensure team are fully informed trained in all of the trials and play a key role to support informed consent to participate, randomising and allocating treatments as required. Act as a resource and support to patients and their relatives, explaining practical aspects of the trial or study, assisting and supporting local nursing teams. Coordinate the collection of all biological samples required as part of the clinical trial/study and ensure safe and appropriate storage of specimens, in conjunction with Sponsors. Ensure the safe administration of trial drugs, have in-depth knowledge of the legal requirements of a clinical trial sponsor regarding pharmacovigilance and of the Trust pharmacovigilance policy. Report any adverse events and reactions in accordance with this policy and the trial protocol. At all times to ensure clear, accurate records are maintained by the team. Implement and adhere to the principles of Good Clinical Practice (GCP) and ensure that all trials are conducted according to the Medicines for Human Use (Clinical Trial) Regulations 2004 and Amended Regulations 2006 where appropriate. Perform tasks requiring highly developed clinical skills including phlebotomy, cannulation and be able to care for patients in the critical care environment. To oversee the routine maintenance and servicing of clinical equipment MANAGEMENT: To act as clinical supervisor to junior research staff and act as a role model for excellence in clinical research. To represent Guys and St Thomas NHS Foundation Trust as an expert research nurse in external situations, for example national and international conferences, committees etc. To report any adverse incident/near misses in relation to that activity To facilitate and maintain effective communication within the clinical team. To responsibly manage the control of equipment, resources and stock through the adherence of research policies and clinical trials budgets. EDUCATION: Ensure mandatory clinical trials training is undertaken and updated as required. To be responsible for developing and sustaining own knowledge, clinical skills and professional awareness. PROFESSIONAL: You will be accountable for your own professional actions, and be a lead specialist for defined area acting within clearly defined policies/procedures and codes of conduct including the NMC code and Trust policy. To act in accordance with local policies and procedures laid down by Guys and St Thomas NHS Foundation Trust and ensure that all mandatory training for nursing staff within the Trust is attended.To work within the NMC Scope of Professional Practice and Code of Conduct. To undertake Performance Development Review annually to identify organisational and professional objectives and developmental needs.To keep up to date with departmental, Trust, NHS, academic and EU developments for the management of clinical research ensuring timely, effective implementation of changes. To attend courses as deemed relevant, including mandatory training, and to attend meetings and conferences as appropriate.

The School of Psychology and Life Sciences (PLS) is a vibrant and diverse community of academics, postgraduate and undergraduate students with approximately 150 academic staff and 30 professional service and technical support staff, providing innovative multidisciplinary science and social science education across a range of both undergraduate and postgraduate programmes to approximately 2000 students. The School is organised into three Sections and you will work within the Section of Natural and Applied Sciences (NAS), joining an energetic and multidisciplinary team of about 20 academic staff. The Section delivers a number of single honours degree programmes that integrate the core sciences (chemistry, physics and biology) including both BSc Biomedical Science and BSc Human Biology pathways. These pathways are currently being updated to include a follow-on taught MSc in Biomedical Science and IBMS accreditation at undergraduate and postgraduate level. In the two most recent National Student Surveys, the Biomedical Science course has achieved results well above benchmark, leading all Universities nationally in most metrics in 2023. The science programmes within the Section are all offered with a foundation (Level 0) entry and the Section also offers an MPhil/PhD in Biological Sciences and an MSc by Research in Biosciences. Our laboratory facilities are based within the University's new £65 million STEM building that houses CCCUs specialist laboratory facilities. Within this STEM building, NAS is located alongside the new Kent and Medway Medical School (KMMS), other lab-based disciplines in PLS, and the new School of Engineering, Technology and Design. We also have a specialist Life Sciences Industry Liaison Lab based at Discovery Park, Sandwich, one of Europe's leading science and technology parks. This Liaison Lab provides industry relevant experience of commercial standard laboratories to students studying courses across the life sciences and facilitates research collaboration with industries based at Discovery Park. The School has an extensive research and knowledge exchange (RKE) portfolio that focuses on the impact of our work on stakeholders. In the last Research Excellence Framework (REF) assessment (REF 2021), the majority of the Schools submitted impact case studies were assessed to be world leading or internationally excellent. This RKE activity contributes to a research-enhanced offer to students that embeds research involvement in the curriculum and allows students to experience first-hand how the subjects and disciplines they are studying make a difference to society, the environment and to peoples lives. The University is growing its capacity in Biomedical Science over the coming years and wishes to appoint an enthusiastic and experienced candidate at Principal Lecturer (teaching and leadership emphasis) or Reader (research and knowledge exchange emphasis) grade in Biomedical Science. To support the delivery of clinical specialism modules for the new IBMS accredited course, we are seeking candidates with extensive practice experience in a clinical setting (e.g. NHS, private healthcare), especially in the areas of haematology, transfusion science, cellular pathology or other clinically relevant areas. The ideal candidate will have had some experience in leadership in a clinical laboratory setting and be on the HCPC (Health and Care Professions Council) register. A PhD is not a required qualification, we will consider applicants with relevant and significant experience in clinical or medical/biomedical practice. If a successful candidate has interest in completing a part-time PhD while in post, this would be supported as far as possible. Some experience of teaching or training practitioners, colleagues or students is essential, but this does not have to be in a higher education context. The successful candidate will have an active involvement in the design, organisation and delivery of the Biomedical Science courses at undergraduate and postgraduate level. They will also support the application of the School for IBMS accreditation of its Biomedical Science course where possible and ideally will be able to support liaising with the NHS and other healthcare providers to provide clinical laboratory placements for students on the new Biomedical Science undergraduate course. In addition to teaching specialist modules, the successful candidate may also on occasion deliver modules or sessions across the wider Natural and Applied Sciences (NAS) curriculum and provide supervision of research project students. The post holder will be a member of the NAS academic team and will work closely with the other members of the team in the planning, delivery, assessment and evaluation of programmes in general.

You will be able to find a full Job description and Person Specification attached within the supporting documents or please click Apply now to view in Trac

Please refer to the job description and person specification for full details of the role. Inclusive Recruitment & Selection We are committed to being an inclusive employer and accurate data capture is an important part of that to ensure we are supportive and representative. Our aim is to ensure that all applicants can see themselves in the available categories on our application form, but we recognise that some of our data capture fields are not inclusive. We have flagged this with our system provider to ask for change. We offer encouragement and active support to applicants with additional needs, including those from ethnic minorities, with disabilities and members of the LGBTQ+ community. If you wish to adjust any aspect of the recruitment process or wish to find out more about our recruitment & selection processes, please get in touch with our Recruitment Manager: Catherine.Gilbert7@nhs.net We are continually reviewing our recruitment & selection process to support the long-term aim of Sheffield Childrens being a champion of Equality, Diversity, and Inclusion. If you have any ideas for improvement, please get in touch with Catherine Gilbert at Catherine.Gilbert7@nhs.net Trust Values The Trust is committed to providing great quality patient care and keep children, young people and families at the heart of what we do by following our CARE values: Compassion leading by kindness and showing empathy, understanding and respect Accountability striving to do the right thing and owning responsibility Respect value differences, tackling inequality and fostering a culture of inclusion Excellence delivering a high-quality standard of care

The post holder is responsible for the management of a defined caseload, namely patients requiring intravitreal injection treatment as part of a multidisciplinary eye care team within medical retina clinics. Flexibility for delivery of subspeciality clinics dependant on experience. The post holder will work to support delivery of induction, specialised training, and educational requirements for all clinical colleagues of eye care services. Supporting Eye Care Services Senior Team to ensure that staff achieve 100% compliance with any Trust mandatory training. The post holder will also be expected to support the safe conduct of research in accordance to the regulatory and legal frameworks related to planning, undertaking and closure of clinical research studies

Please see attached job description and person specification to support your application for this post. Please refer to the essential criteria in the person specification which will highlight the skills, knowledge and experience you will need to demonstrate in your application, by way of example, to give yourself the best opportunity to be shortlisted. The main duties and responsibilities consists of: Working closely with research members to contribute to the delivery of the improvement science research programme. Being responsible for study design, recruitment and data collection and analysis. Obtaining necessary ethical and governance approvals at project outset. Conduct literature searching. Provide regular progress reports. Writing blogs to help promote the theme and our findings, writing publications (as the lead or a co-author) and other dissemination activities that will help to optimise the impact of our work. Be involved in grant applications and to supervise more junior staff members. Applying for NHS research ethics committee approval. Qualitative data collection and analysis. Literature searching. Recruitment of participants. Management of data. To engage with colleagues within the Young Peoples Mental Health Research Centre and the Trust Research Innovation team offering advice and guidance as required. To work effectively with patients, the public and healthcare staff to ensure our research meets the needs of these groups. To be involved with research publications and conference abstracts. To ensure that research governance procedures and GDPR legislation is adhered to. To enhance the impact of our work through engagement with professional conferences, writing for different audiences, blogs, short course development, etc. To undertake personal development in keeping with the aspiration to be a national leader in health research. To update the theme manager on project progress and outcomes to enable monitoring for and reporting to the NIHR. Lead on designing projects. To manage and/or mentor more junior staff. To lead on or contribute to funding opportunities.

Please see attached Job Description and Person Specification. To apply, please click APPLY FOR THIS JOB - this link will take you to the TRAC Recruitment Site. You will need to register if you do not already have an account As an employer and sponsor licence holder, to be able to provide sponsorship to overseas nationals via the Skilled Worker route we must ensure that we adhere to the sponsorship requirements set by UK Visas and Immigration. After carefully reviewing this role, we do not believe that this position meets the requirements for sponsorship. For details on eligibility criteria for a Skilled Worker visa, please follow this link to the gov.uk website Skilled Worker visa: Overview - GOV.UK (www.gov.uk)

The post holder will be responsible for the project management of clinical research trials, working closely with the the research project delivery team to deliver an array of studies across multiple specialties, on and off site. This will require the deployment of administrative, analytical and interpersonal skills, management of study finances, occasional processing of participant samples and effective communication at all levels of the organisations involved. Experience in project management is essential. Planning and co-ordinating approval processes required for implementing new trials in liaison with Research Delivery Business Manager and R&D. Co-ordinate and manage relationships with all stakeholders involved in research projects Facilitate all non-clinical aspects of a clinical trial from set up to completion Support with patient screening, acquisition of trial data, management, submission and related administration including the management of study level finances. Facilitating supply of office and trial consumables. Assists in preparation and appropriate processing of patient samples as per protocol, in laboratory setting.

PLEASE REFER TO THE ATTACHED JOB DESCRIPTION FOR FULL DUTIES OF THE ROLE. Support the COLOSPEED studies including COLOCOHORT. Responsibility for study related medical support within own expertise and in consultation with study Principle Investigators (PIs). Liaison with the wider hospital teams such as laboratories, radiology, endoscopy, critical care, pain team, infection control, palliative care and oncology. Assist in the training and development of medical and nursing staff on study requirements. Ensure studies are delivered in accordance with good clinical practice and study protocols. Participate in research meetings. Take part in other responsibilities deemed responsible by their supervisor. Assist in the development of study protocols, grant applications and publications as directed by supervisor. Register and obtain an MD or PhD from Newcastle University.

For further information on this role, please see the attached detailed Job Description and Person Specification. To assess and evaluate the progress of on-going clinical trials and research undertaken in the unit, maintaining an accurate account of the status of the projects and to regularly update the department on the status To assist with the organisation and implementation of clinical trials, and liaising closely with the multi-disciplinary team to facilitate a co-ordinated approach to patient care. To ensure that proposed research projects for which the post-holder has responsibility are registered and reviewed by the Trusts R & D department and Research Ethics Committee (REC) prior to commencement and that updates and amendments are reported in a timely fashion. To liaise with pharmaceutical sponsors regarding feasibility and implementation aspects of proposed clinical trials To liaise with the multidisciplinary team to promote and oversee the appropriate referral and recruitment of patients to research trials within the unit for which the post holder has a designated responsibility. To ensure the safe administration of all treatments and drugs that are given within the context of a clinical trial To act as a support for patients and relatives throughout the trial, providing information as well as physical, spiritual and emotional support where necessary, and referring to other healthcare professionals where appropriate To participate in Trust wide education programmes, study days, courses, meetings or conferences as identified in their Personal Development Plan and deemed appropriate for their professional development by their line manager. Ensure performance issues are dealt with in an appropriate and timely manner and follow the Trust's Disciplinary or Capability Procedures where formal action is necessary.

For full duties and responsibilities please refer to the attached document entitled Job Description.

Health and physical abilities sufficient for the post (if necessary with reasonable adjustments with respect to the Equality Act/Disability Discrimination Act). Qualifications / training required GCSE level A to C or equivalent in at least two from Maths, English and Science ECDL or equivalent knowledge of computers Previous knowledge of hospital IT systems NVQ Level 2 (Clinical Laboratory Support) Previous or relevant experience necessary Previous experience in laboratory work. Previous experience in an NHS environment. Previous experience as a laboratory support worker Aptitudes and skills required Keyboard skills Literate and numerate Articulate Able to follow laboratory procedures Attention to detail Special requirements of the post To work flexible hours as determined by the needs of the service Work and remain calm under pressure to meet daily deadlines Able to work as a member of a team or on own initiative Enthusiastic, motivated Values and behaviours Able to demonstrate behaviours that meet the Trust Values Patients First Always Improving Working Together