Total 23 science rd research job vacancies in le1

Science Teacher Job - Leicester

Start date: ASAP
Position: Science Teacher
Location: Leicester-based Secondary School

You must have relevant experience working with 11 -16-year-olds within the last 2 years, and we must be able to obtain relevantreferences for this time. You should have a professional manner and a flexibleattitude to working and timetable changes. Most importantly, you should beenthusiastic, engaging and passionate about working with young people. Strongbehaviour management and the ability to implement schools' behaviour polices isalso essential.

Job Description:

• Delivering engaging and creative Science lessons to students in Key Stages 3 and 4.
• Planning and preparing schemes of work, lesson plans, and assessments.
• Monitoring student progress and providing feedback.
• Contributing to the development of the department's curriculum.
• Participating in extracurricular activities such as school trips.

Requirements:

• Qualified Teacher Status (QTS) or equivalent. ECT's welcome to apply.
• Bachelor's degree in science or related field.
• Recent experience teaching Science at secondary school level.
• Strong behaviour/classroom management.
• The ability to work collaboratively with other teachers and staff members

If you are interested in thisrole, click 'apply now' to forward an up-to-date copy of your CV.

Alternatively, if this job isn'tquite right for you, but if you are looking for a new position, please contact usfor a confidential discussion about your career. Hays also offer a greatRefer-A-Friend Scheme worth £350 in high street vouchers!

Hays Specialist Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at hays.co.uk

To assist with the acquisition and distribution of relevant trial documentation. To assist with the acquisition and distribution of study equipment/tools and ensure relevant health and safety checks are carried out in accordance with relevant Trust Policies. To assist in the preparation and submission of documentation for clinical research approvals. To create and maintain trial site files for each trial in accordance with ICH-GCP and Research Governance. Collection of patient data from medical notes and completion of case record form (CRF) and to liaise with clinical trials coordinators, research nurses and investigators to ensure accurate data collection. To transcribe/export data from medical records (paper or electronic) to CRFs (paper or electronic e-CRFs) as required by the study protocol. To ensure safe filing and storage of study documentation in accordance to research governance. Conduct quality assurance of documentation. To organise and prepare for visits by trial monitors as required by the study protocol. To take responsibility for liaising with clinical trial units regarding data queries and for checking and resolving data queries. To support the assessment of patient eligibility, in liaison with other appropriate health care professionals for clinical trial entry, involving coordination of pre study tests, obtaining results and arrangingappropriate appointments as per clinical trial protocol. To provide written and verbal information relevant to the research study and support clinical staff in the process of gaining informed consent from participants that are entering into clinical research. To deal with telephone enquiries from staff, patients and relatives, ensuring that appropriate personnel are informed in order for actions to be taken. To report any adverse events to the appropriate research nurse and/or principal investigator (PI). Presenting specific trial information at multidisciplinary team meetings. To act in a professional manner at all times when dealing with patients, relatives and representatives from both within and outside of the Trust. Co-ordination of specified trials and take responsibility for : Organisation of any necessary tests and investigations as detailed within the Sample preparation (e.g. blood, urine, tissue and faecal samples): retrieval, centrifuging, pipetting, slide making and preparation for storage, liaising with the hospital and external laboratories when appropriate. Undertaking low risk clinical duties. Maintaining logs of stored samples and freezer temperatures. Maintaining adequate stock levels of sample kits. Required to hold a phone for a short period of time to monitor freezer/fridge temperatures including during and out of office hours. Organising the logistical aspects of diagnostic specimens, packaging, and shipment, including handling of dry ice. Resolving data queries raised by sponsoring organisations. Archiving all study related material including patients notes after study closure. Reporting and submitting of Serious Adverse Events (SAEs) from this site within stipulated timeframes to sponsor organisations and the Research and Innovation Office. Tracking Serious Unexpected Event reporting. Maintaining and updating study specific site files. Notifying General Practitioners of their patients involvement in a clinical trial. As a new post holder, training will be provided for the key aspects of this role, and a period of induction identified, however, the post holder will be expected to take advantage of opportunities to upgrade their skills and to attend meetings and workshops to enhance their knowledge.

This is a unique and exciting opportunity to join the Research & Innovation (R&I) workforce at University Hospitals of Leicester (UHL).

This is a great opportunity to become a member of the HOPE cancer trials team. We have an ever changing diverse portfolio of clinical haematology and oncology trials including those exploring compounds at the early stages of development. We offer a commitment to support training and professional development needs and the opportunity to develop interests and skills in the prevention, diagnosis and treatment of cancer.

There are close relationships between the Biomedical Research Centre (BRC) Themes, University of Leicester and UHL clinical areas across the 3 sites. Funding from the Clinical Research Network (CRN) will support the delivery of research programmes across all specialties at UHL.

The appointee’s main responsibilities include collecting, recording and maintaining data for patients and volunteers on research studies. To support research staff in ensuring the completeness, accuracy and consistency of the data in order to meet standards expected for reporting to regulatory bodies.

To provide support in clinical trials such as preparing, handling and processing biological samples, and data management and resolution, in accordance with the clinical trial protocol and Good Clinical Practice (GCP). To ensure compliance with UHL policies on data protection, confidentiality and security.

The post holder will provide the highest standards of patient care in line with research protocols and ICH Good Clinical Practice guidelines, safeguarding the well-being and safety of the patients and integrity of the data.

To work alongside Principal Investigators and the research team to assist in the delivery of a high quality research service of clinical expertise, professional advice, support, guidance and education to the multi-professional team, patients and carers within the research service.

The post-holder will ensure the highest standard is delivered to research subjects and, where relevant to their families, in partnership with all members of the multi professional and research teams.

We are one of the biggest and busiest NHS trusts in the country, incorporating the General, Glenfield and Royal Infirmary hospitals. We have our very own Children’s Hospital and run one of the country’s leading heart centres.

Our team is made up of more than 17,000 staff providing a range of services primarily for the one million residents of Leicester, Leicestershire and Rutland.

We work with partners at the University of Leicester and De Montfort University providing world-class teaching to nurture and develop the next generation of doctors, nurses and other healthcare professionals, many of whom go on to spend their working lives with us.

Our purpose is to provide ‘Caring at its best’ and our staff have helped us create a set of values that embody who we are and what we’re here to do.

Our patients are at the heart of all we do and we believe that ‘Caring at its best’ is not just about the treatments and services we provide, but about giving our patients the best possible experience.

About the University Hospitals of Leicester NHS Trust (leicestershospitals.nhs.uk)
• To assist with the acquisition and distribution of relevant trial documentation.
• To assist with the acquisition and distribution of study equipment/tools and ensure relevant health and safety checks are carried out in accordance with relevant Trust Policies.
• To assist in the preparation and submission of documentation for clinical research approvals.
• To create and maintain trial site files for each trial in accordance with ICH-GCP and Research Governance.
• Collection of patient data from medical notes and completion of case record form (CRF) and to liaise with clinical trials coordinators, research nurses and investigators to ensure accurate data collection.
• To transcribe/export data from medical records (paper or electronic) to CRFs (paper or electronic e-CRFs) as required by the study protocol.
• To ensure safe filing and storage of study documentation in accordance to research governance.
• Conduct quality assurance of documentation.
• To organise and prepare for visits by trial monitors as required by the study protocol.
• To take responsibility for liaising with clinical trial units regarding data queries and for checking and resolving data queries.
• To support the assessment of patient eligibility, in liaison with other appropriate health care professionals for clinical trial entry, involving coordination of pre study tests, obtaining results and arranging appropriate appointments as per clinical trial protocol.
• To provide written and verbal information relevant to the research study and support clinical staff in the process of gaining informed consent from participants that are entering into clinical research.
• To deal with telephone enquiries from staff, patients and relatives, ensuring that appropriate personnel are informed in order for actions to be taken.
• To report any adverse events to the appropriate research nurse and/or principal investigator (PI).
• Presenting specific trial information at multidisciplinary team meetings.
• To act in a professional manner at all times when dealing with patients, relatives and representatives from both within and outside of the Trust.
• Co-ordination of specified trials and take responsibility for :• Organisation of any necessary tests and investigations as detailed within the
• Sample preparation (e.g. blood, urine, tissue and faecal samples): retrieval, centrifuging, pipetting, slide making and preparation for storage, liaising with the hospital and external laboratories when appropriate.
• Undertaking low risk clinical duties.
• Maintaining logs of stored samples and freezer temperatures.
• Maintaining adequate stock levels of sample kits.
• Required to hold a phone for a short period of time to monitor freezer/fridge temperatures including during and out of office hours.
• Organising the logistical aspects of diagnostic specimens, packaging, and shipment, including handling of dry ice.
• Resolving data queries raised by sponsoring organisations.
• Archiving all study related material including patient’s notes after study closure.
• Reporting and submitting of Serious Adverse Events (SAEs) from this site within stipulated timeframes to sponsor organisations and the Research and Innovation Office.
• Tracking Serious Unexpected Event reporting.
• Maintaining and updating study specific site files.
• Notifying General Practitioners of their patient’s involvement in a clinical trial.
• As a new post holder, training will be provided for the key aspects of this role, and a period of induction identified, however, the post holder will be expected to take advantage of opportunities to upgrade their skills and to attend meetings and workshops to enhance their knowledge.


This advert closes on Thursday 31 Oct 2024

Please refer to the Application Pack, detailed Job Description and Person Specification for further information.

1.1 Work alongside clinical colleagues across CMGs delivering research education practice and evidence-based practice in clinical care. 1.2 Take a lead role in the facilitation and provision of research education and professional practice and expertise for staff whilst working in defined / allocated clinical area. 1.3 Participate in the development, implementation and delivery of competency based research practice education, supervision and assessment of staff in the practice setting. 1.4 Contribute to Trust wide core training delivering research practice such as Preceptorship, registrant Induction, OSCE Programme, Healthcare Support Worker Induction 1.5 Promote high quality clinical care and assist in the development and expansion of practice that meets the needs of the service and user. 1.6 Actively contribute to the support of leaners, supervisors and assessors within the clinical area to enrich the quality of their research learning experience. 1.7 Actively contribute to the education and training of Healthcare Support Workers acknowledging their growing contribution to the delivery of care in the clinical area. 1.8 Maintain clinical credibility and visibility by working in the practice setting in the support of clinical colleagues, care of patients when and where it is appropriate to the role. 1.9 To contribute to the local implementation of the UHL Induction and Study Leave Policies and the UHL Nursing, Midwifery and AHP Strategy For more details please refer to the Job Description

In partnership with the University of Leicester, the Institute for Excellence in Healthcare (IEH) aims to deliver world-class research opportunities for healthcare colleagues in Leicester, Leicestershire and Rutland. The IEH aims to develop new opportunities to help embed research in day-to-day clinical practice whilst growing as a Centre of Excellence for research. The IEH is committed to growing capacity and capability in research, education and innovation. Supported by a team of experts, you will play a pivotal role in shaping the future of UHL and partners organizations at local, regional and national level.









The post-holder will:

· Work with the IEH and the UHL Education and Practice Development Team to identify relevant research education and training needs to support the development and delivery of an innovative Trust wide education and training programme aimed at enhancing research competencies across UHL

· Engage with the clinical areas in Research awareness promoting and delivering education in research practice.

· Contribute to the development of the IEH research infrastructure to support local implementation of the IEH research objectives.

Work in close collaboration with the Education and Practice Development Team to ensure that the clinical areas provide a positive practice environment in research practice for new starters, students and learners.

Our new strategy, developed with the support and feedback of colleagues, patients, and partners, is our compass for the next seven years (2023-2030).

We have four primary goals:
• high-quality care for all,
• being a great place to work,
• partnerships for impact, and
• research and education excellence

And we will embed health equality in all we do - taking active steps to reduce the avoidable differences in healthcare that some people face, working in partnership with communities.

Our strategy is underpinned by new values and we will work to ensure they are an everyday reality for all:
• we are compassionate,
• we are proud,
• we are inclusive, and
• we are one team

This is an exciting moment as we look to the future with clarity on what we already do well and where we need to focus our energies to make an even bigger difference for the people we serve.

About the University Hospitals of Leicester NHS Trust:

http://www.leicestershospitals.nhs.uk/aboutus/work-for-us/current-vacancies/

1.1 Work alongside clinical colleagues across CMGs delivering research education practice and evidence-based practice in clinical care.

1.2 Take a lead role in the facilitation and provision of research education and professional practice and expertise for staff whilst working in defined / allocated clinical area.

1.3 Participate in the development, implementation and delivery of competency based research practice education, supervision and assessment of staff in the practice setting.

1.4 Contribute to Trust wide core training delivering research practice such as Preceptorship, registrant Induction, OSCE Programme, Healthcare Support Worker Induction



1.5 Promote high quality clinical care and assist in the development and expansion of practice that meets the needs of the service and user.

1.6 Actively contribute to the support of leaners, supervisors and assessors within the clinical area to enrich the quality of their research learning experience.

1.7 Actively contribute to the education and training of Healthcare Support Workers acknowledging their growing contribution to the delivery of care in the clinical area.

1.8 Maintain clinical credibility and visibility by working in the practice setting in the support of clinical colleagues, care of patients when and where it is appropriate to the role.

1.9 To contribute to the local implementation of the UHL Induction and Study Leave Policies and the UHL Nursing, Midwifery and AHP Strategy

For more details please refer to the Job Description


This advert closes on Sunday 20 Oct 2024

Teacher of Science - Maternity cover

• West Leicestershire based secondary school
• To start in January 2025
• Full-time and long-term position
• Teaching Science at KS3 and KS4

We are working in partnership with an Ofsted 'Good' Secondary school in West Leicestershire who are seeking an enthusiastic and committed Science Teacher to join their team in November. This is a full-time and long-term role to cover maternity leave. Due to this being a long-term role, full teaching responsibilities will be required, including planning and marking.

Job Description:

• Delivering engaging and creative science lessons to students in Key Stages 3 and 4.
• Planning and preparing schemes of work, lesson plans, and assessments.
• Monitoring student progress and providing feedback.
• Contributing to the development of the department's curriculum.
• Participating in extracurricular activities such as sports clubs and school trips.

Requirements:

• Qualified Teacher Status (QTS) or equivalent. ECT's welcome to apply.
• Bachelor's degree in a science or related field
• Recent experience teaching Science at secondary school level.
• Strong behaviour/classroom management.
• Ability to work collaboratively with other teachers and staff members

If you are interested in this role, click 'apply now' to forward an up-to-date copy of your CV. Alternatively, if this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.

If you know someone looking for a new teaching position please let us know, as Hays offer a great Refer-A-Friend Scheme worth £350 in high street vouchers!

We look forward to hearing from you.

Hays Specialist Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at hays.co.uk

Manages a personal caseload of clinical trials and patients independently with minimal supervision/mentoring from Principle Investigators/senior research nurses/team leaders. To ensure relevant approvals are in place prior to commencing each trial. To ensure all work is undertaken in line with the research protocol, ICH-GCP and Research Governance guidelines. To act as one of the primary points of contact for clinical trials patients. To educate other staff as to the responsibilities of the role and function of the research nurse and disseminate information on specific studies. Observe patients and monitor treatment/toxicity side effects; escalating findings accordingly. To maintain Professional Accountability for nursing research practice at all times Identifies, screens and recruits patients for the clinical trial using agreed protocols in accordance with ICH-GCP and Research Governance Provides education and support for patients in research trials Work with the lead clinician to evaluate clinical trial proposals, identifying potential patient populations and evaluating cost implications of the trial. Work with the R&I Co-ordinator to ensure all clinical trial documentation has appropriate ethical committee and Trust approval providing feedback to the lead clinician and research directorate. Participate in set-up/initiation/monitoring visits, site audits and study close-down meetings carried out by sponsoring organisations and regulatory authorities. Provide on-going audit reports as required by the trial protocols and Research & Innovation department/ethics committee. Responsible for resolving data queries raised by sponsoring organisations. Demonstrates commitment to the role of patient advocate for patients considering or participating in clinical trials. To provide mentorship and supervision for other research professionals and staff within and outside the department. Act as a resource for ward based nurses wishing to undertake research once competencies have been achieved. Responsible for assisting with the completion of study costing templates along with assisting with invoicing and the recovery of income for commercial research as per financial contract agreement. please see job description/person specification for further details on the role

We currently have an exciting opportunity for a haematology and oncology clinical research nurse.

The Hope Cancer Trials centre research team are looking for an individual with excellent communication skills who is resourceful, organised and a flexible team player with an eye for detail.

This post holder will support our portfolio of haematology and oncology studies. Ideally you will have a good understanding of the principles of clinical research. However, applications from candidates with relevant clinical experience who demonstrate enthusiasm and commitment to develop their knowledge and skills in this specialist area will be considered.

Depending on the relevant experience we would offer the role as either a Band 5 or Band 6. The Band 5 will have the opportunity to develop to a Band 6 through the agreed milestones.

Although based at Leicester Royal Infirmary, cross-site working may be required, with the potential to work cross-speciality if required. The successful candidate will be supported by the wider research team, link in with the multi-disciplinary team and have links with other research teams.

If you think you have the attributes that we are looking for and share our vision of developing our research portfolio for the benefit of patient care, then come and join our team
• The appointee’s main responsibilities will include providing senior skilled nursing care to ensure the safe and efficient running of research studies within the designated facility. This includes ensuring the research has full approval to proceed; screening and recruiting participants, collecting data and data entry.
• The appointee will also identify barriers to recruitment and assist in finding solutions to overcome these.
• To be responsible for the assessment of care needs and the development, implementation and evaluation of care, using agreed frameworks.
• To manage and participate in the co-ordination of research studies within the facility and provide research skills and senior clinical care for patients undergoing investigations.
• The role requires the development and maintenance of clinical practice skills and competencies including venepuncture, cannulation, IV and oral drug administration (including SACT), analysis of blood samples, vital signs measurements, Basic Life Support/ILS and other advanced skills as required for specific studies.
• The post holder will provide the highest standards of patient care in line with research protocols and will ensure that such research safeguards the well-being of the patients and is conducted within ICH Good Clinical Practice guidelines for research.

Our new strategy, developed with the support and feedback of colleagues, patients, and partners, is our compass for the next seven years (2023-2030).

We have four primary goals:
• high-quality care for all,
• being a great place to work,
• partnerships for impact, and
• research and education excellence

And we will embed health equality in all we do - taking active steps to reduce the avoidable differences in healthcare that some people face, working in partnership with communities.

Our strategy is underpinned by new values and we will work to ensure they are an everyday reality for all:
• we are compassionate,
• we are proud,
• we are inclusive, and
• we are one team

This is an exciting moment as we look to the future with clarity on what we already do well and where we need to focus our energies to make an even bigger difference for the people we serve.

About the University Hospitals of Leicester NHS Trust:

http://www.leicestershospitals.nhs.uk/aboutus/work-for-us/current-vacancies/
• Manages a personal caseload of clinical trials and patients independently with minimal supervision/mentoring from Principle Investigators/senior research nurses/team leaders.
• To ensure relevant approvals are in place prior to commencing each trial.
• To ensure all work is undertaken in line with the research protocol, ICH-GCP and Research Governance guidelines.
• To act as one of the primary points of contact for clinical trials patients.
• To educate other staff as to the responsibilities of the role and function of the research nurse and disseminate information on specific studies.
• Observe patients and monitor treatment/toxicity side effects; escalating findings accordingly.
• To maintain Professional Accountability for nursing research practice at all times
• Identifies, screens and recruits patients for the clinical trial using agreed protocols in accordance with ICH-GCP and Research Governance
• Provides education and support for patients in research trials
• Work with the lead clinician to evaluate clinical trial proposals, identifying potential patient populations and evaluating cost implications of the trial.
• Work with the R&I Co-ordinator to ensure all clinical trial documentation has appropriate ethical committee and Trust approval providing feedback to the lead clinician and research directorate.
• Participate in set-up/initiation/monitoring visits, site audits and study close-down meetings carried out by sponsoring organisations and regulatory authorities.
• Provide on-going audit reports as required by the trial protocols and Research & Innovation department/ethics committee.
• Responsible for resolving data queries raised by sponsoring organisations.
• Demonstrates commitment to the role of patient advocate for patients considering or participating in clinical trials.
• To provide mentorship and supervision for other research professionals and staff within and outside the department.
• Act as a resource for ward based nurses wishing to undertake research once competencies have been achieved.
• Responsible for assisting with the completion of study costing templates along with assisting with invoicing and the recovery of income for commercial research as per financial contract agreement.

please see job description/person specification for further details on the role


This advert closes on Thursday 29 Aug 2024

The role will involve acquiring and maintaining an in depthknowledge of trial protocols, research methodologies and therequirements of local, national and international researchregulation to provide, safe ethical practice.To develop and maintain constructive working relationship with themulti-professional teams within the service. Be a facilitator forgood communication within the service. Actively participate in localand national networking groups to develop an expert level ofknowledge. Clinical Practice:The research Nurse will: Have an understanding of the application of ICH GCPGuidelines, the EU Directive on Clinical Research andResearch Governance. Identify patients suitable for entry into clinical trials andresearch studies. This may include attending clinics andmultidisciplinary team meetings, reviewing medical notesand inclusion/exclusion criteria. Ensure patients / carers are provided with writteninformation relevant to the research study and are giventhe opportunity to discuss the research study or clinical trialadequately at the outset and during the course of theresearch or clinical trial in which they are being asked toparticipate (i.e. informed consent). Attend and support patients in the clinical environment formonitoring, assessment and follow up as part of researchprojects. Where appropriate, take consent frompatients/participants to enter research studies. Take relevant patient samples for clinical trials; such asblood samples, to centrifuge and separate serum, packageand dispatch as per defined protocols, where appropriate. Observe patients and monitor treatment toxicity/sideeffects; escalating findings accordingly. The Research Nurse will be responsible for thecoordination and support given to researchers in order to completeresearch Capacity and Capability assessments in order to obtainR&I Authorisation for research studies they wish to conduct.Keeping abreast of legislation, the post-holder will also beresponsible for implementing national best practice researchmanagement processes within the Trust. They will be responsiblefor ensuring that local integration of systems and processes areachieved so that individuals can benefit fully from this in astreamlined manner.The Research Nurse will be responsible foridentifying and addressing Trust specific feasibility issues andensuring that studies are reviewed, set up and submitted for R&Iauthorisation in a timely manner and resourced appropriately.The post-holder will be the day to day point of contact forinvestigators and will be responsible for providing advice andsupport ensuring that they have full access to the range of thehigh quality research management functions in order to securesuccessful completion.The post holder should be adaptable, flexible and show initiative.In addition they need to show good communication skills, be ableto liaise with all levels of staff, demonstrate good organisationalskills and attention to detail and have good time managementskills.Opportunities to develop expertise in other research specialtieswill be available. The post-holder may be required to work in otherresearch areas across UHL if service needs arise.

A very exciting opportunity has arisen for an experienced practitioner to join the Clinical Research Team at the NIHR Leicester Clinical Research Facility (CRF) Research Space based in our Microbiology/Infection/Critical care and Emergencies and Injuries teams (ICE). We are a friendly and dedicated team of multi disciplinary professionals committed to providing the highest quality of patient care and research.

The Research Space is busy and very successful at recruitment to a diverse portfolio of research studies and trials mainly within secondary care.

We are seeking to appoint a band 6 Clinical Research Nurse , with the appropriate level of experience and qualifications to join us in our dynamically developing team.

The successful applicant will provide support for the multi-disciplinary Research team and be part of our management structure helping to develop junior and new staff.

As well as being personable, they will have excellent communication skills and be a strong team-player, enabling them to deal with patients directly and liaise with colleagues at all levels. In addition to working within the team they will be expected to have the ability to use their own initiative. Training will be given where required.





Research Management and Governance

Information Management

Communication and Relationship Skills

Participant wellbeing

Training and Education

Identify learning needs of self and other staff and assist the Senior Research Nurse in the relevant training in relation to clinical trial set up and conduct





Our new strategy, developed with the support and feedback of colleagues, patients, and partners, is our compass for the next seven years (2023-2030).

We have four primary goals:
high-quality care for all,
being a great place to work,
partnerships for impact, and
research and education excellence.

And we will embed health equality in all we do - taking active steps to reduce the avoidable differences in healthcare that some people face, working in partnership with communities.

Our strategy is underpinned by new values and we will work to ensure they are an everyday reality for all:
we are compassionate,
we are proud,
we are inclusive, and
we are one team

This is an exciting moment as we look to the future with clarity on what we already do well and where we need to focus our energies to make an even bigger difference for the people we serve.

About the University Hospitals of Leicester NHS Trust:

http://www.leicestershospitals.nhs.uk/aboutus/work-for-us/current-vacancies/

The role will involve acquiring and maintaining an in depth
knowledge of trial protocols, research methodologies and the
requirements of local, national and international research
regulation to provide, safe ethical practice.
To develop and maintain constructive working relationship with the
multi-professional teams within the service. Be a facilitator for
good communication within the service. Actively participate in local
and national networking groups to develop an expert level of
knowledge.

Clinical Practice:
The research Nurse will:
· Have an understanding of the application of ICH GCP
Guidelines, the EU Directive on Clinical Research and
Research Governance.
· Identify patients suitable for entry into clinical trials and
research studies. This may include attending clinics and
multidisciplinary team meetings, reviewing medical notes
and inclusion/exclusion criteria.
· Ensure patients / carers are provided with written
information relevant to the research study and are given
the opportunity to discuss the research study or clinical trial
adequately at the outset and during the course of the
research or clinical trial in which they are being asked to
participate (i.e. informed consent).
· Attend and support patients in the clinical environment for
monitoring, assessment and follow up as part of research
projects.

Where appropriate, take consent from
patients/participants to enter research studies.
· Take relevant patient samples for clinical trials; such as
blood samples, to centrifuge and separate serum, package
and dispatch as per defined protocols, where appropriate.
· Observe patients and monitor treatment toxicity/side
effects; escalating findings accordingly.

The Research Nurse will be responsible for the
coordination and support given to researchers in order to complete
research Capacity and Capability assessments in order to obtain
R&I Authorisation for research studies they wish to conduct.
Keeping abreast of legislation, the post-holder will also be
responsible for implementing national best practice research
management processes within the Trust. They will be responsible
for ensuring that local integration of systems and processes are
achieved so that individuals can benefit fully from this in a
streamlined manner.
The Research Nurse will be responsible for
identifying and addressing Trust specific feasibility issues and
ensuring that studies are reviewed, set up and submitted for R&I
authorisation in a timely manner and resourced appropriately.
The post-holder will be the day to day point of contact for
investigators and will be responsible for providing advice and
support ensuring that they have full access to the range of the
high quality research management functions in order to secure
successful completion.
The post holder should be adaptable, flexible and show initiative.
In addition they need to show good communication skills, be able
to liaise with all levels of staff, demonstrate good organisational
skills and attention to detail and have good time management
skills.
Opportunities to develop expertise in other research specialties
will be available. The post-holder may be required to work in other
research areas across UHL if service needs arise.


This advert closes on Sunday 4 Aug 2024

Promotion of the CRN East Midlands Research Site Initiative (RSI) Scheme, and contribution to the overall growth of research conducted in Health, Social and Primary Care in your locality. Performance management of the RSI sites against key performance indicators for the financial year Promotion of Research within Primary Care, this may include presentations to healthcare professionals/ providers and the general public.Supporting research nave Health, Social and Primary Care sites in becoming research active, this may include assisting with the delivery of research training and education Maintain an understanding of the changing landscape in Health, Social and Primary Care, with specific focus on Primary Care Networks (PCNs) Work with the CRN Study Support Service to support the facilitation of study set-up and delivery in Primary Care settings, the post holder will be expected to collaborate effectively, and engage with a diverse range of personnel including: staff members from primary care organisations, R&D staff, commercial/non-commercial sponsoring and funding organisations, chief/principle investigators (academic and NHS), heads of department, directorate leads, and staff from other Trusts. Utilising and updating the Local Performance Management System Edge, in the performance management of Primary Care sites and studies. Promoting and utlising the CRN East Midlands Primary Care Research Website and supporting sites to access and use this. Assisting sites in keeping site Research Activity Records up to date. To develop an understanding of the application of ICH GCP Guidelines, the EU Directive on Clinical Research and Research Governance. To work alongside Health, Social and Primary Care sites, ensuring staff delivering research at the sites have in date ICH GCP and Informed Consent (where appropriate) training. The following duties may be undertaken by the post holder, at times when there is a requirement for additional clinical delivery support for studies taking place in the region: To identify patients suitable for entry into clinical trials and research studies, this may include attending clinics and multidisciplinary team meetings, reviewing medical notes and inclusion/exclusion criteria. To ensure patients / carers are provided with written information relevant to the research study and are given the opportunity to discuss the research study or clinical trial adequately at the outset and during the course of the research or clinical trial in which they are being asked to participate (i.e. informed consent) To attend and support patients in the clinical environment for monitoring, assessment and follow up as part of research projects. Where appropriate, to take consent from patients/participants to enter research studies. To take relevant patient samples for clinical trials; such as blood samples, to centrifuge and separate serum, package and dispatch as per defined protocols, where appropriate. Observe patients and monitor treatment toxicity/side effects; escalating findings accordingly. Maintain accurate patient trial documentation, complete Case Record Forms, including the use of electronic data capture systems and ensure relevant information is recorded in patients medical notes. Ensure safety data is reported to required SOPs and study protocols, and reports sent in a timely manner. To ensure safe and appropriate storage of specimens, in accordance with the trial protocol and in conjunction with specialist teams. To record and report any adverse events and serious adverse events according to trial protocol and local procedures. Develops and maintains constructive relationships whilst reconciling or resolving conflict. Be responsible for managing their own workload, working to competing deadlines, working against performance targets and resolving problems. Takes responsibility for implementing decisions and plans owned by the team. Maintain efficient and effective communication with Primary Care Team Leader on issues related to staff conduct within research trials and impact on participant care. To be flexible in their approach to work as the role may require flexibility in terms of timing e.g. for specific treatments. In accordance with professional codes, maintain own professional development and competence to practice. Undertake data entry and assure its accuracy and timeliness to study records in both LPMS (Edge) and national (CPMS) databases and support their maintenance. Create of reports on study setup and patient recruitment, using the Open Data Platform and other NIHR Systems and use these to review data quality and to support performance monitoring and management of studies. Provide CRN assistance to audits, monitoring visits or regulatory inspections. Take responsibility for the maintenance of confidentiality, security and integrity of information relating to patients, staff and other health service members in the NHS organisation and IHSP setting of the Study Support Service. Provide research support and training for individual trials being conducted within the network region, it is expected that this will involve working on more than one project at any time and in more than one clinical specialty as appropriate. Develop training guides as required to support researchers and colleagues in understanding aspects of the Primary Care Research Delivery Team. Ensure that training pertinent to the role is up to date e.g. ICH-GCP, Edge, as well as mandatory training as directed to develop/maintain skills and knowledge. Be flexible in the approach taken to work. Be accountable for all tasks within the scope of the role and to be aware of developmental needs/limitations while providing support to others. As the post will cover a number of NHS Trusts/partner organisations, there will be a requirement to travel around the geographical area covered by the CRN: East Midlands on a frequent basis.

General Responsibilities To ensure timely and accurate input of follow-up data into electronic forms and databases. Work with the research team to resolve data queries. Help facilitate the completion of questionnaires. Take responsibility for maintaining and managing (creating, storing and updating) spreadsheets of patient recruitment to studies and providing information from a recorded source. Maintain and help to facilitate the process of archiving study documents. Attend any relevant meetings regarding the conduct and close down of clinical trials. Co-ordinate, prepare and participate in monitoring visits, site audits and study close down meetings carried out by sponsoring organisations and authorities which govern clinical trials. Prepare research-related paperwork and documents as required. This may relate to any part of the research process. Minute taking for meetings as required. Maintaining and updating all essential documents in the Research Investigator Site Files. Work in line with the research protocol, International Conference of Harmonisation Good Clinical Practice and Research Governance guidelines. Support members of the Research Team in the implementation and maintenance of research projects. Assist in the preparation and despatch of samples and documents to professionals within the hospital and external organisations. Obtain samples and undertake sample preparation (blood, urine, tissue and faecal samples); to include centrifuging, pipetting, preparation for storage, liaising with hospital and laboratory staff as appropriate Maintaining logs of stored samples and freezer temperatures To deal with telephone enquiries, ensuring that appropriate personnel are informed so that actions to be taken. Liaise with staff across the hospital for issues that relate to research. Assist staff and visitors with their enquiries. Ensure that all work is undertaken according to hospital policies and regulations which cover clinical trials. To provide support as requested and to undertake any other appropriate duties as required.

Science Teacher job - Leicester

• Start date: September
• End date: Until Christmas with the potential to extend
• Position: long term Science teacher position
• Location: Leicester-based secondary school

We are working in partnership with an Ofsted 'Good' Secondary school in Leicester who are seeking an enthusiastic and committed Science Teacher to join their team at the start of the new academic year. This is a full-time and long-term job until Christmas with the potential to extend. Due to this being a long-term role, full teaching responsibilities will be required, including planning and marking. To be successful, you will have recent experience teaching Science to KS3 and KS4. ECTs are welcome to apply.

Job Description:

• Delivering engaging and creative science lessons to students in Key Stages 3 and 4.
• Planning and preparing schemes of work, lesson plans, and assessments.
• Monitoring student progress and providing feedback.
• Contributing to the development of the department's curriculum.
• Participating in extracurricular activities such as sports clubs and school trips.

Requirements:

• Qualified Teacher Status (QTS) or equivalent. ECT's welcome to apply.
• Bachelor's degree in science or related field
• Recent experience teaching Science at secondary school level.
• Strong behaviour/classroom management.
• Ability to work collaboratively with other teachers and staff members

If you are interested in this role, click 'apply now' to forward an up-to-date copy of your CV.

Alternatively, if this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career. Hays also offer a great Refer-A-Friend Scheme worth £350 in high street vouchers!

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Job description uploaded. Key duties include: Recruitment & consent of research patients Completion of trial activities Data collection Sample processing Resolving queries (Please refer to the job description/person specification for further details on the role)