Total 18 science rd research job vacancies in coventry cv2 2dx

Paediatric role will require working at City of Coventry Health Centre and University Hospital Coventry and Warwickshire. Adult role will require working at Rugby St Cross and University Hospital Coventry and Warwickshire Closing Date: Please be advised that this job advert will close as soon as sufficient applications have been received. Please apply for this job as soon as you can, if interested. For further details please see the attached job description.

As outlined in the Job Description, this roles key responsibilities include supporting the delivery of antimicrobial stewardship, medicines management, and research activities, all while contributing to the quality of patient care across the Trust. You will work to implement antimicrobial initiatives, ensure accurate and timely dispensing, and assist in research projects that enhance our understanding and management of infection control. Additionally, youll play a crucial role in identifying development needs and creating opportunities for technical and support staff to advance their skills, ensuring our pharmacy team is prepared to provide exceptional service. For further details, please refer to the attached Job Description.

The interview date for shortlisted applicants for this role is the 10th September 2024 . For further details of the role please see the attached job description.

1. Support the Lead Nurse of R&D with ensuring service objectives are met and deputising for lead nurse as required. 2. Responsible for the efficient management of processes e.g. complaints within research, training and development; appraisal and patient recruitment. Undertake bleep-holder responsibilities for R&D as required. 3. Utilise information and IT systems to produce accurate and timely workforce and resource data and reports. 4. Responsible for development, implementation and evaluation of projects to improve patient care and service development through the audit cycle, linking to the clinical governance and research governance frameworks and business planning process. 5. Undertake occasional direct workload requiring moderate to high physical effort according to patient dependency or staff need. 6. Demonstrate through effective leadership the ability to provide professional and emotional support to individuals and groups, e.g. during difficult situations or unexpected events. 7. Accountable for maintaining a clean, safe environment ensuring adherence to Trust standards of cleanliness, hygiene and infection control at all times.8.Responsible for adherence to Health and Safety and Trust policy and Divisional objectives designed to protect healthcare staff and service users from clinical and non-clinical risk and known hazards. If you are interested in this opportunity and wish to discuss further please contact Nicolas Aldridge Lead Nurse for R&D or Ceri Jones Head of R&D. To apply please find the application on TRAC. For further details of the role please see the attached job description.

a) To interpret laboratory results and take appropriate actions in line with service policies. b) Give technical information to other service users such as appropriate specimens/sampling and turnaround times. c) Contribute to project set up, recruitment, and project delivery planning. d) Assist in the review of project/study protocols and contribute to feasibility/project selection process, advising on regulatory and logistical issues. e) Work with other teams and investigators to develop strategies to overcome barriers to recruitment/collection and solve other problems relating to specific projects. f) Provide information to project participants/patients regarding their participation in order to facilitate effective informed consent. g) To undertake informed consent ensuring that consent forms are completed accurately and filed as required and in accordance with HTA regulation. h) Co-ordinate the recruitment of patients to research projects in addition to oversight of junior team members participation. i) Work unsupervised in all areas related to the research projects and supervise junior team members. j) Collect relevant samples as required by the research project, package and dispatch as required. Ensure safe and appropriate storage of specimens in accordance with HTA regulations and Trust guidance. k) To coordinate/organize hosted collections and supervise/support junior members of the team. For further details of the role please see the attached job description.

A range of clinical investigations, procedures or processes can be performed to deliver patient care according to the agreed IMP. These investigations, procedures or processes must also be interpreted and reported to the patient and others involved in his/her care. The following may be undertaken: audiometry, diagnostic tympanometry; diagnostic reflexes; OAEs; speech audiometry. Paediatric assessments the following may be undertaken: VRA testing, distraction testing, play or performance audiometry and PTA. Paediatric testing will be led by a Specialist Healthcare Science Practitioner (Audiology) / Healthcare or Clinical Scientist. Within the role of the Practitioner, further skill development is possible and expected with a view to further advancement. For further details of the role please see the attached job description.

The post holder will be employed by the Research and Development Department (R&D) to work within the Midwifery research team predominantly, though there may be a need to work flexibly across several research speciality teams as service requirements dictate. They will contribute to the provision of a clinical research service based normally at the location of the employing organisation (UHCW NHS Trust); however, travel to other sites may be required as per study requirements or set out under contractual agreements for the delivery of a local cross cutting clinical research service. Support Research Midwives, Nurses and Physicians by assisting in the planning and conduct of all types of research studies. Adhere to trial protocols and work in accordance with ICH GCP and Trust Standard Operating Procedures. Manage and co-ordinate own portfolio of uncomplicated studies, not requiring qualified medical/ nursing intervention in accordance with the relevant Local, National and International guidelines. Use databases to access patient groups to improve patient opportunity and recruitment to trials. Identify/screen patients for studies and registers/ enrol patients into these studies, ensuring informed consent is in place. Co-ordinate and manage a portfolio of non-interventional research studies in line with protocol ethics approvals. Coordinate the follow up of an identified caseload of trial patients with minimal supervision. Day to day maintenance of patient records whilst the trial is in progress, data entry onto electronic or paper based case records forms. Assist in the preparation of and participate in monitoring visits, and respond to data queries. Ensure serious adverse events are reported and acted upon as required by the protocol in liaison with a research nurse and or Principle Investigator For further details of the role please see the attached job description.

Clinical Ensure care to patients is delivered according to Trust policies and procedures and the research protocol. Co-ordinate the care of own case load of clinical trial / research patients in addition to oversight of junior team members caseloads Work unsupervised in all areas related to clinical trials and research studies and supervise the work of junior team members Attend Multi-disciplinary Meetings, and appropriate clinics, to assess volunteers/patients for eligibility for research and recruit new patients, to act as a resource to the members of the MDT. Communicate information regarding clinical decisions to patients, carers and the MDT as required Ensure that trial specific clinical investigations / procedures are undertaken as required by the research protocol in order to establish eligibility and maintain safety in the trial Take relevant samples as required by the study protocol such as blood samples, package and dispatch as defined. Ensure safe and appropriate storage of specimens in accordance with trial protocols and regulatory / Trust guidance With relevant training and assessment of competence, working within scope of professional practice, undertake clinical procedures / administer treatments associated with the research treatment regimes Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial. Monitor treatment toxicity/side effects reporting to the relevant personnel, recording as required assisting in any required changes to treatment as required by the protocol. For further details please see the attached for further details.

The Arden Centre is equipped with five Elekta linacs, SGRT, an orthovoltage treatment machine, Elekta HDR brachytherapy and RayStation treatment planning system. We have a modern portfolio of techniques including a growing SABR service. The Arden Centre is located on the University Hospital site at Walsgrave which is on the edge of historic Coventry with convenient transport to the City and easy access to rural Warwickshire, the M6 and the M69 motorways. Part time and flexible working arrangements including moderate working from home can be accommodated. We are an accredited training department at all levels of medical physics including HSST. Main duties: 1. To act as lead Medical Physics Expert in Radiotherapy Physics research. This means acting as a lead source of knowledge and expertise in this field, to interpret measured and predicted results and determine the reasons for anomalous results and the cause of subtle or non-reproducible equipment or technique faults. 2. Research and Development:2.1. To assist with the strategic development of programmes of research in Clinical Physics and Biomedical Engineering, supporting those who seek external funding.2.2. To manage the portfolio of Radiotherapy Physics research and clinical trials activity.2.3. To foster and coordinate links with academic institutions.2.4. To promote and facilitate joint research between UHCW and the West Midlands Radiotherapy Network.2.5. To initiate, supervise and carry out research in Radiotherapy Physics seeking external funding where appropriate.2.6. To report on the results of such research at national and international scientific meetings and by published papers in refereed journals. 3. Management3.1. To undertake interviews, appraisals and personal progress reviews as delegated by the Head of Radiotherapy Physics.3.2. To procure equipment and services relevant to specialist area.3.3. To monitor and report to the Head of Radiotherapy Physics on the non-staff budget for the relevant specialist area of radiotherapy physics.3.4. To deputise for the Radiotherapy Physics Operational Lead in his/her absence.3.5. To co-ordinate the work of the department for the relevant specialist area of radiotherapy physics. For further information on this post, please refer to the job description and person specification attached.

Individual Management Plan (IMP) Development The development of the IMP should include a range of investigations, procedures or processes in consultation with families and relevant others, based on the individual child's needs and wishes and accepted good practice. The IMP should be monitored and progress reported, reviewing the need for further intervention as appropriate. Develops and delivers IMPs for families within specialist Audiology services e.g. paediatrics Diagnostic Assessments The Advanced Healthcare Scientist in Audiology undertakes the full range of available Audiological tests unsupervised, including advanced diagnostic testing, in particular, frequency specific objective testing to determine thresholds in young babies. Auditory Rehabilitation The Advanced Audiologist develops interventions and rehabilitation programmes based upon autonomous clinical opinion, which may involve onward referral to relevant intervention programmes such as specialist tertiary services. The rehabilitation programmes may also include balance rehabilitation; tinnitus rehabilitation; paediatric habilitation.In addition the Specialist Audiologist may undertake motivational interviewing or counselling. The Specialist Audiologist has an awareness of local external agencies who can provide additional help and support to the patient and will signpost/refer the patient as agreed For further details of the role please see the attached job description.

Clinical Work autonomously to manage a caseload of patients acting as a professional to ensure care to patients is delivered according to Trust policies and procedures and the research protocol delivery high standards and continuity of clinical care for study participants. Maintain strong relationships and communication channels with other key personnel such as multidisciplinary teams, clinical wards areas. Attend Multi-disciplinary Meetings, and appropriate clinics, to assess volunteers/patients for eligibility for research and recruit new patients, to act as a resource to the members of the MDT. Ensure that trial specific clinical investigations / procedures are undertaken as required by the research protocol in order to establish eligibility and maintain safety in the trial by all team members. Take relevant samples as required by the study protocol such as blood samples, package and dispatch as defined. Ensure safe and appropriate storage of specimens in accordance with trial protocols and regulatory / Trust guidance. Ensure all team members undertake relevant training and assessment of competence, working within scope of professional practice prior to undertaking any clinical procedures / administration of treatments associated with the research treatment regimes. Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial by all team members. Ensure staff monitor treatment toxicity/side effects reporting to the relevant personnel, recording as required assisting in any required changes to treatment as required by the protocol Ensure all staff record and report adverse /serious adverse events as classified in the study protocol criteria which occur whilst patient is in the clinical trial e.g. hospital admission since last study visit Ensure accurate documentation of patients events in nursing/medical notes and study specific case report forms. Provide ongoing information, education and support to patients (and their significant others) regarding clinical trials and their care. Research and Portfolio Management Lead in the delivery of studies within the relevant specialities ensuring they meet the requirements with regards to the Department of Healths Research Governance Framework for Health and Social Care and the EU Clinical Trials legislation by implementing quality systems. Assist in the review of study protocols and contribute to the feasibility/study selection process, advising on safety, regulatory and logistical issues. Liaise with RD&I Set Up Team staff contributing to the process of gaining local regulatory committee approval where required to ensure efficient service is delivered to sponsors. Work with the research teams and investigators to develop strategies to overcome barriers to recruitment and solve other problems relating to specific studies. Following appropriate training and competence assessment receive written informed consent from participants for allocated research studies in accordance with study protocol and Trust guidance. Following appropriate training and competence assessment act as an assessor for the process of informed consent for research according to Trust guidelines. Randomise / enrol patients into clinical trials or other research studies. Assess and evaluate the progress of on-going clinical trials and research identifying resource implications for the teams. Co-ordinate the monthly local portfolio team performance meetings: identify and act on issues. Ensure accurate records for all research projects that are overseen within allocated teams are kept in accordance with all regulatory requirements including the data protection act Ensure that all ICH GCP required documentation is kept in a clearly traceable system and is stored in an appropriate manner for the appropriate length of time. Provide advice and support to other members of the research and multidisciplinary team with regard to research governance. Ensure self and team members respond to data queries generated by the study co-ordinating team within a timely manner. Ensure all team members maintain accurate records of study recruitment as per local procedure and status of studies providing regular updates. This will involve ensuring that EDGE (local patient management system) is updated with key trial data and feeding back through the local portfolio team meetings For further details please see the attached job description.

The successful candidate will have a relevant health / mental health related degree or qualification. They should be computer literate, with excellent communication, interpersonal and organisational skills. Knowledge of and experience of health and/or social care research is essential. The role will involve travel to research sites across Coventry and Warwickshire so applicants must have the ability to move freely across the Trust.

The successful candidate will have a relevant health / mental health related degree or qualification. They should be computer literate, with excellent communication, interpersonal and organisational skills. Knowledge of and experience of health and/or social care research is essential. The role will involve travel to research sites across Coventry and Warwickshire so applicants must have the ability to move freely across the Trust.

To assist with the implementation and maintenance of efficient office management systems and procedures to enable our team to optimise their standards of service. This will require effective time management, arranging and preparation and maintenance of correspondence and reports, manipulation of documentation management systems and general workflow tasks. To support team members with research funding applications. This will require undertaking appropriate staff training and development as required, confidently providing cross-cover on a reciprocal basis in the absence of colleagues. Searching for funding and development opportunities and providing support to new and existing researchers is a core element of being effective in this role. To use initiative and work to standard operating procedures and working instructions to meet essential work requirements and to achieve accurate data capture from researchers in relation to research funding applications, research outputs and other metrics according to reporting requirements. This will require being able to learn and maintain the best practices in the capture of technical, scientific and research data and metrics, being flexible to changing needs.

Clinical Work autonomously to manage a caseload of patients acting as a professional to ensure care to patients is delivered according to Trust policies and procedures and the research protocol delivery high standards and continuity of clinical care for study participants. Maintain strong relationships and communication channels with other key personnel such as multidisciplinary teams, clinical wards areas. Attend Multi-disciplinary Meetings, and appropriate clinics, to assess volunteers/patients for eligibility for research and recruit new patients, to act as a resource to the members of the MDT. Ensure that trial specific clinical investigations / procedures are undertaken as required by the research protocol in order to establish eligibility and maintain safety in the trial by all team members. Take relevant samples as required by the study protocol such as blood samples, package and dispatch as defined. Ensure safe and appropriate storage of specimens in accordance with trial protocols and regulatory / Trust guidance. Ensure all team members undertake relevant training and assessment of competence, working within scope of professional practice prior to undertaking any clinical procedures / administration of treatments associated with the research treatment regimes. Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial by all team members. Ensure staff monitor treatment toxicity/side effects reporting to the relevant personnel, recording as required assisting in any required changes to treatment as required by the protocol Ensure all staff record and report adverse /serious adverse events as classified in the study protocol criteria which occur whilst patient is in the clinical trial e.g. hospital admission since last study visit Ensure accurate documentation of patients events in nursing/medical notes and study specific case report forms. Provide ongoing information, education and support to patients (and their significant others) regarding clinical trials and their care. Research and Portfolio Management Lead in the delivery of studies within the relevant specialities ensuring they meet the requirements with regards to the Department of Healths Research Governance Framework for Health and Social Care and the EU Clinical Trials legislation by implementing quality systems. Assist in the review of study protocols and contribute to the feasibility/study selection process, advising on safety, regulatory and logistical issues. Liaise with RD&I Set Up Team staff contributing to the process of gaining local regulatory committee approval where required to ensure efficient service is delivered to sponsors. Work with the research teams and investigators to develop strategies to overcome barriers to recruitment and solve other problems relating to specific studies. Following appropriate training and competence assessment receive written informed consent from participants for allocated research studies in accordance with study protocol and Trust guidance. Following appropriate training and competence assessment act as an assessor for the process of informed consent for research according to Trust guidelines. Randomise / enrol patients into clinical trials or other research studies. Assess and evaluate the progress of on-going clinical trials and research identifying resource implications for the teams. Co-ordinate the monthly local portfolio team performance meetings: identify and act on issues. Ensure accurate records for all research projects that are overseen within allocated teams are kept in accordance with all regulatory requirements including the data protection act Ensure that all ICH GCP required documentation is kept in a clearly traceable system and is stored in an appropriate manner for the appropriate length of time. Provide advice and support to other members of the research and multidisciplinary team with regard to research governance. Ensure self and team members respond to data queries generated by the study co-ordinating team within a timely manner. Ensure all team members maintain accurate records of study recruitment as per local procedure and status of studies providing regular updates. This will involve ensuring that EDGE (local patient management system) is updated with key trial data and feeding back through the local portfolio team meetings For further details please see the attached job description.