Total 23 science rd research job vacancies in Liverpool, Merseyside, L3 9SJ

Following appropriate induction and under direction and supervision, to undertake protocol based psychological assessments of clients including standard psychometric tests, self-report measures, rating scales, direct and indirect structured observations and semi-structured interviews with clients, family members and others involved in the clients care. To assist in the delivery of care plans involving the psychological treatment and / or management of a clients problems, under the supervision of a qualified professional psychologist. The post holder can be required to work in highly emotive atmosphere and must maintain a high degree of professionalism at all times. To assist in the co-ordination and running of therapeutic groups. To work with other staff to assess outpatients and inpatients and review their care in preparation for multi-disciplinary reviews. To assist in the development of a psychologically based framework of understanding and care to the benefit of all clients of the service, across all care settings. To attend and contribute to clinical psychology meetings and appropriate multidisciplinary meetings, as directed by the qualified clinical psychologists.

Clinical To co-ordinate the care and support of their own case load of clinical trial participants To attend multidisciplinary team meetings and act as a resource to members of the MDT Undertake extended roles in relation to the demands of the individual studies. To screen potential participants and assess patient eligibility for clinical trial entry To approach parents to introduce and discuss the study and to approach parents to gain informed consent after they have had time to consider the study To co-ordinate trial treatments, obtaining relevant supplementary data and arranging appropriate appointments as necessary according to the clinical trial protocol to ensure patient safety To attend appropriate clinics to promote study participation and screen and recruit new participants To ensure the safe administration of treatments and drugs given within the context of a clinical trial To ensure blood and/or other samples are collected and transported as required by the trial protocol To ensure that trial specific investigations are undertaken as required by the protocol To clinically assess and evaluate patients on the trial To maintain accurate, comprehensive and legible patient notes (written and electronic) of all clinical events in accordance with the Trust and national professional policies and guidelines To monitor and maintain accurate written and/or computer records with regards to physical and psychological changes/ treatment toxicity and side effects experienced by patients and taking appropriate action To record and report all adverse events that occur as part of the clinical trial in accordance with the protocol and delegated responsibilities To provide ongoing support and follow up care for the child and family whilst the child is in the clinical trial To carry out follow up checks and interventions as detailed in the trial protocol which may occasionally require visits to other sites or to patients own homes To collect follow up data from other wards according to the study protocol To act as a primary contact point (for trial issues) for the child and family for the duration of the trial To adhere to clinical departmental policies at all times Work in collaboration with other members of the multidisciplinary team to ensure the family and child fully understand the nature of the trial; his/her voluntary entry to the trial and freedom to withdraw at any time without prejudice to treatment Research To be responsible for the operational management of the study in accordance with the UK Policy Framework for Health and Social Care Research 2018, ICH Good Clinical Practice (ICH GCP), the Caldicott Guardian, Medicines for Human Use (Clinical Trials) Regulations, Data Protection Act 1998 and other local policies and procedures. To work alongside clinicians and other nurses to develop strategies to overcome barriers to recruitment To assist with the recruitment and randomisation if appropriate of eligible children into the clinical study To facilitate the informed consent of a participant (appropriate to age and understanding) during the recruitment process in accordance with ICH GCP and other guidelines To be responsible for forwarding study data in a timely manner to the trial co-ordinating centre when requested and in accordance with the trial protocol To accurately document data collected into the case report forms (CRF) To assist in the maintenance of the trial databases, ensuring that all reporting of data is documented and stored in the correct manner To provide support to the Principal Investigator(s) to ensure that study data is appropriately archived To keep the Principal Investigator, other appropriate members of the trial team informed of the progress of the trial, supplying data to them as required To be aware of ethical considerations of research and act as the patients advocate at all times To be fully conversant and compliant with the requirements of the clinical trial protocol in relation to patient management, data collection and safety reporting To work closely with and in support of the Principle Investigator(s) and other Research Personnel involved in all aspects of the trial To ensure data is accessed in accordance with both the Data Protection Act and the Caldicott Guardian Education and Training To act as a resource for local staff at participating sites in relation to clinical trials To maintain an awareness of current advances in paediatric treatments, research and nursing practice within the relevant speciality To continue professional development, keeping updated with current clinical practice to maintain professional registration To maintain links with other trial nurses to develop and share knowledge and to provide mutual support To attend local and national meetings/training events as deemed necessary for the role, including mandatory GCP training To identify, assess and meet the educational needs of the patient and the family to facilitate understanding and compliance with the trial protocol To provide teaching to members of clinical staff on the trial protocol procedures and items of equipment deemed necessary for the purposes of the trial Communication To provide highly specialised advice to patients and their families concerning the care and treatment during participation in the trial To provide information and education in a way that is suitable for the child, their carers and families, including the manner in which the information is disseminated, complexity and language used and the timing of its giving To be responsible for maintaining strong relationships and positive communication channels with all participating members of the study and staff involved To ensure all communication is evidenced and documented as required by governance standards Other To understand and adhere to local Trust policies and procedures. To act in accordance with the NMC Professional Code of Conduct The post holder has responsibility for safety as outlined in the hospitals policy and Health and Safety Work Act 1974 To maintain confidentiality at all times To comply with the Research Governance Framework 2005 To work alongside other research staff assigned to the study and other related studies as deemed appropriate and provide complementary support to the research team To maintain confidentiality at all times

To disseminate information to colleagues in respect of the research studies taking place within the clinical areas. Liaison with research sponsors and multi-disciplinary research teams. To give advice on the organisation and management of the research in progress. To identify and screen eligible patients for participation in the research studies. To facilitate the informed consent and recruitment of research participants. To work with staff to develop strategies to overcome barriers to recruitment. To be aware of ethical considerations of research and act as the patients advocate at all times. To be fully conversant with the requirements of the clinical trial protocol in relation to patient management, data collection and safety reporting. To carry out the collection, processing and shipping of biological specimens according to protocol requirements and follow-up appropriately. Maintain accurate records and undertake the Data management including the use of data software packages. Dissemination and publication of research findings. Actively contribute to activities, events and training within the research teams. To contribute to evidence based practice at a clinical level and maintain overall standard of care for patients at all times.

To disseminate information and educate colleagues in respect of research within the Trust. Liaison with Trust and and multi-disciplinary research teams. To give advice on the organisation and management of the research in progress. To identify and screen eligible patients for participation in the project. To facilitate the informed consent and recruitment of research participants. To work with staff to develop strategies to overcome barriers to recruitment. To be aware of ethical considerations of research and act as the patients advocate at all times. To be fully conversant with the requirements of the project protocol in relation to patient management, data collection and safety reporting. Maintain accurate records and undertake the data management including the use of data software packages. To assist with dissemination and publication of research findings. Actively contribute to activities, events and training within the research team. To contribute to evidence based practice at a clinical level and maintain overall standard of care for patients at all times. To act as a resource for local staff at the participating site in relation to research projects. To keep appropriate staff informed of the progress of research projects. To maintain an awareness of current advances in research and midwifery practice. To continue professional development, keeping updated with current clinical practice to maintain professional registration. To maintain links with other research midwives across the network to develop and share knowledge and to provide mutual support. To attend local and national meetings in relation to research as required.

The post holder is responsible for the safe and effective management of the research nursing service Lead and manage personnel providing opportunities for staff development, which meets the identified core needs of the ward through empowerment and progression planning. Implement a robust system of performance management to ensure all staff undergo training and development to meet core skills. Ensure patient flow is effective and timely through clinical research study set and management Demonstrate through clinical practice the required role model for all staff grades. Adhere to and facilitate Trust Risk Management Strategy at local level. Maintain and monitor departmental budget through effective resource management systems with the support of the Lead Clinical Research Nurse/Matron. Ensure self and staff adhere to Trust/Department professional development programmes. Ensure staff participation in Trust events and follow up action plans to implement effective change management across the division. Ensure staff participation in service developments. Manage staff performance ensuring high clinical standards are maintained utilising review systems such as appraisal and professional development plans which reflect competencies. Participate in the relevant Clinical Research Network meetings networking with other Research Units Ensure the nurses are compliant with relevant Clinical Research Facility (CRF) Standards as outlined by the NIHR CLINICAL RESPONSIBILITIES Lead clinical practice ensuring the delivery of a high standard of family centred care Manage staff performance to ensure high clinical standards are maintained utilising review systems such as appraisal and professional development. Ensure patients privacy is maintained and religious and cultural beliefs are respected at all times. Promote and maintain a safe, comfortable and therapeutic environment for patients, staff and families. Be responsible for ensuring quality care delivery within the CRF and by the clinical research nursing staff through the audit of nursing practice and implementation of evidence based clinical research. Promote effective communication to ensure a cohesive and seamless approach to care. Responsible for ensuring that performance data is recorded effectively in order to monitor and evaluate activity within the ward area. Responsible for performance management and obtaining Key performance indicators within the clinical research nursing service. Facilitate the partnership approach between patient, parents and all professionals involved in their care, to provide a positive patient experience. To participate / undertake risk management assessments at local level and develop strategies to improve quality care, this would include clinical risks and RCA. EDUCATION AND TRAINING Will ensure own professional and / or clinical training needs are identified and any core deficits addressed, within a 12 month time frame, meeting agreed learning action plan deadlines with the support of the Lead Clinical Research Nurse/Matron Develop and facilitate educational and training programmes for the nursing team to ensure compliance with mandatory, statutory and specialist clinical skills. Facilitate / lead nursing staff development through clinical and academic support. Ensure nurse training is compliant with relevant Research Governance and CRF standards. RESEARCH: Lead / Promote and participate in the Trusts / National Benchmarking program thus improving quality and standards of care. Support and facilitate Trust research projects through implementation of the research strategy within the Unit. . Continually update own knowledge. Actively promote and support Quality Audits at both local and Trust level in order to improve standards of care. Participate and lead as appropriate CRF Patient Safety Scans. QUALITY ASSURANCE: Monitor and further develop standards of care for children cared for on the CRF and by the clinical research nursing team. Undertake risk management assessments ensuring robust action plans are adhered to. Work towards National Guidelines and DOH incentives. Undertake patient/parent satisfaction surveys as directed by the Trust. Participate in Trust quality review assessments. PROFESSIONAL DEVELOPMENT Continue to develop self and role through clinical supervision/action learning and continuing professional education. Attend yearly mandatory training sessions and participate in Trust programmes.

Please see attached Job Description and Person Specification for full details about this exciting role on offer at The Clatterbridge Cancer Centre. Please carefully read the essential and desirable criteria and ensure you can demonstrate how you meet the requirements for this role.

To disseminate information to colleagues in respect of the research studies taking place within the clinical areas. Liaison with research sponsors and multi-disciplinary research teams. To give advice on the organisation and management of the research in progress. To identify and screen eligible patients for participation in the research studies. To facilitate the informed consent and recruitment of research participants. To work with staff to develop strategies to overcome barriers to recruitment. To be aware of ethical considerations of research and act as the patients advocate at all times. To be fully conversant with the requirements of the clinical research study protocol in relation to patient management, data collection and safety reporting. To carry out the collection, processing and shipping of biological specimens according to protocol requirements and follow-up appropriately. Maintain accurate records and undertake the data management including the use of data software packages. Dissemination and publication of research findings. Actively contribute to activities, events and training within the research teams. To contribute to evidence based practice and maintain overall standard of care for patients at all times.

Liaising with investigators, researchers, external organisations and sponsors. Collect and record on the EDGE database information in respect of research projects being undertaken. Arranging meetings, seminars, research courses etc and distribution of information to investigators and other relevant staff. To provide administrative support to meetings, eg production of meeting minutes To provide administrative support with site file maintenance. To provide clinical research teams with support eg data input into research study CRF systems and databases, sending GP letters, scheduling research participants appointments, making recruitment packs, stock management. Maintain the research section of the Trusts internet, intranet and social media pages, keeping them up to date with current information. Responsible for the collation of information for and production of the RD&I newsletter Manage the RD&I department generic research email, actioning incoming emails and referring to the most appropriate individual. To manage the process of archiving research documentation To collate research information to support clinicians revalidations/appraisals. General office duties including, but not limited to, filing, photocopying, ordering of supplies, dealing with general enquiries Co-ordinate and prioritise own workload and tasks commensurate with providing adequate administrative support

To disseminate information to colleagues in respect of the research studies taking place within the clinical areas. To identify and screen eligible patients for participation in the research studies. To facilitate the informed consent and recruitment of research participants. To assist with the development of strategies to overcome barriers to recruitment. To be aware of ethical considerations of research and act as the patients advocate at all times. To be fully conversant with the requirements of the clinical research study protocol in relation to patient management, data collection and safety reporting. To carry out the collection, processing and shipping of biological specimens according to protocol requirements and follow-up appropriately. Maintain accurate records and undertake the data management including the use of data software packages. Actively contribute to activities, events and training within the research teams. To contribute to evidence based practice and maintain overall standard of care for patients at all times.

To disseminate information and educate colleagues in respect of the project within the Trust. Liaison with Trust, Genomics England and multi-disciplinary research teams. To give advice on the organisation and management of the research in progress. To identify and screen eligible patients for participation in the project. To facilitate the informed consent and recruitment of research participants. To work with staff to develop strategies to overcome barriers to recruitment. To be aware of ethical considerations of research and act as the patients advocate at all times. To be fully conversant with the requirements of the project protocol in relation to patient management, data collection and safety reporting. Maintain accurate records and undertake the data management including the use of data software packages. To assist with dissemination and publication of research findings. Actively contribute to activities, events and training within the research team. To contribute to evidence based practice at a clinical level and maintain overall standard of care for patients at all times. To act as a resource for local staff at the participating site in relation to the project. To keep appropriate staff informed of the progress of the project. To maintain an awareness of current advances in research and midwifery practice. To continue professional development, keeping updated with current clinical practice to maintain professional registration. To maintain links with other research midwives across the network to develop and share knowledge and to provide mutual support. To attend local and national meetings in relation to research as required.

The post holder will support, lead, supervise, manage and co-ordinate all Research Nurses/Clinical Support Staff within a Portfolio. They will provide a high quality, effective, safe, specialist and clinical trials/research service. We are looking for an individual with excellent leadership qualities, who can motivate and supervise ensuring high standards of patient care throughout the research process. Interview date 31st July 2024.

1 Key Responsibilities 1.1 Providing sample reception support to all disciplines within laboratory medicine and within specific work areas as required. 1.2 Carrying out analytical processes under the supervision of Biomedical Scientists (BMS) to provide a diagnostic service. 1.3 Receiving, collating and performing the preliminary processing of a variety of patient specimens for biomedical analysis, acting on any issues with unlabelled or mislabelled samples as required. 1.4 Manually pipetting plasma/urine samples prior to appropriate storage or analysis. 1.5 Dealing with reception and telephone queries from various Trust staff, GPs and visitors to the department. 1.6 Organising own day-to-day work, prioritising urgent and emergency workloads. 1.7 Perform clerical tasks such as inputting patient demographics and input/retrieval of test request details on laboratory IT systems. 1.8 Operating the pneumatic pod system and ensuring performance issues are reported. 1.9 Identifying and processing high risk/ infectious specimens safely and appropriately. 1.10 Prompt referral of non-routine issues to senior staff. 1.11 Perform general housekeeping including the cleaning of centrifuges, glassware and work surfaces; and the preparation of disinfectant for use. 1.12 Maintaining the safe and confidential storage and retrieval of records and specimens, both physically and electronically. 1.13 Processing and sending away samples to reference laboratories. 1.14 Attending meetings and maintaining an up to date knowledge of new developments in the laboratory. 1.15 Complying with Trust and Departmental Health and Safety policies; reporting accidents, hazards and defects as soon as possible. 1.16 Assisting in completing incident reporting forms when incidents or errors are identified eg mislabelled or incorrect samples. 1.17 Proposing changes and contributing towards improving working practices, turnaround times and SOPs (standard operating procedures) 1.18 Use of expensive complex equipment and where appropriate performing preventative maintenance in accordance with manufacturers instructions and local SOPs 1.19 Ensuring the proper and efficient use of consumables without wastage, performing stock checks and alerting the senior staff when stock levels are low. 1.20 Checking the delivery hub regularly, signing for deliveries and assisting in the distribution and storage of deliveries and stock according to departmental material management policies. 1.21 Performing Quality Control tests. 1.22 Dispense and collect liquid nitrogen following completion of safety training. 1.23 To undertake water flushing requirements 1.24 Participate in late shifts.

Please see attached Job Description and Person Specification for full details about this exciting role on offer at The Clatterbridge Cancer Centre.

You will work closely with the Trust Service Delivery Teams, Sponsors and NIHR CRN NWC. If you are looking for a challenging and exciting opportunity we look forward to hearing from you.

Facilitation of Research Sponsorship unblinded monitoring Line management of small team Protocol review and ethical submission support