Total 67 science rd research job vacancies in coventry cv22dx

Cardinal Wiseman Catholic School

Teacher of Science

MPS/UPS

Required from September 2024

"Cardinal Wiseman School is a happy place to be, where students behave well, achieve well and enjoy learning."

We are seeking an inspirational Teacher of Science to join Cardinal Wiseman Catholic School. This is an exciting time to be part of a growing team as we strive for academic excellence for all students in our care.

We have recently been awarded 'Good' in our last Ofsted Inspection and senior leaders have established an ambitious, knowledge-rich curriculum where students experience the very best knowledge in Science teaching.

This is an ideal opportunity for an ECT or an experienced teacher seeking a new challenge. Teachers receive high quality support and training to develop their practice and are well supported within the school to enable students to achieve their full potential. For a suitable candidate a TLR can be discussed based on skills and experience.

If you are a passionate and motivated teacher who is focused on helping students develop a deep subject knowledge in order to achieve their true potential, we would welcome your application.

In return we can offer:

• a supportive leadership team and vibrant professional community
• quality training to those new to the career from our team of dedicated mentors
• a commitment to continuing professional development
• a positive school culture which believes in distributed and collaborative leadership
• energetic and enthusiastic students
• a supportive, Catholic ethos across our school communities.

Visits to the school are welcomed and encouraged, please get in touch to arrange this.

For further details and an application form please contact Paul Hunt at Hays Education:
M: 07921583731
E:

We are committed to safeguarding and promoting the welfare of our students. All offers of employment will be subject to an enhanced DBS checks.

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

The post holder will be responsible for the day to day management of several of the R&D clinical research studies and teams. The post holder will be supporting the safe conduct of research in accordance with the regulatory and legal frameworks relating to the planning, undertaking and closure of research studies providing assurance that the rights and well being of trial participants are protected.

Excellent support from the close-knit management team will be provided including a comprehensive induction package and the opportunity to really develop as a manager and leader of a patient focused, quality driven, cutting-edge service.

The post holder will be instrumental in implementing team objectives to enhance the performance and development of the research teams whilst providing guidance, education, leadership and co-ordinating the portfolio of research studies and clinical trials to deliver high quality research and clinical care.

The role integrates both clinical duties such as maintaining an active caseload and managerial duties; as such the post holder will be required to effectively manage their time to fulfil key responsibilities. It is also expected that the post holder will be flexible with hours of work as required to ensure that we are offering a service that best suits the needs of our patients.

The post holder will be employed by Research and Development department (R&D) to work within the central clinical research teams of Accident and Emergency, Critical care and Trauma and Orthopaedics, managing an allocated number of research teams.

However, it is expected that the post folder will work flexibly across other research speciality areas as service requirements dictate throughout the duration of their contract.

The post holder will be responsible for the day to day management of several of the R&D clinical research studies and teams. The post holder will be supporting the safe conduct of research in accordance with the regulatory and legal frameworks relating to the planning, undertaking and closure of research studies providing assurance that the rights and well being of trial participants are protected.

The job holder may be required to carry out other similar or related duties within their bounds of registration which do not fall within the work outlined which may reasonably be required to deliver a comprehensive research service to our patients. The Line Manager, in consultation with the post holder will undertake any review.

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.

University Hospitals Coventry and Warwickshire NHS Trust, rated as good by the Care Quality Commission, is one of the largest teaching Trusts in the UK.

We are extremely proud of our employees across our hospital sites, with high quality patient care at the heart of everything we do.

Boasting some of the most modern facilities in Western Europe, the Trust is renowned for being at the forefront of research and innovation as part of its blossoming reputation as a worldwide leader in healthcare.

We are proud to be recognised as a Pathway to Excellence®designated organisation – please click the link for further details about this prestigious award.Pathway To Excellence ® - University Hospitals Coventry & Warwickshire (uhcw.nhs.uk)

By joining our exciting journey, you will form part of a passionate, talented team and will be able to access a wide range of learning and development opportunities. There has never been a better time to join our team.

The Trust is committed to building an organisation that makes full use of the talents, skills, experience, and different perspectives available in our diverse society. We want everyone to feel they are respected, valued, can achieve their potential and receive the most appropriate and relevant care. We will create an environment where the equality and human rights principles of fairness, respect, equality, dignity and autonomy are promoted and are part of the organisation's core values.

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 patient’s 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 Health’s 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.


This advert closes on Monday 27 May 2024

A Vacancy at University Hospitals Coventry and Warwickshire NHS Trust.


Clinical Scientist /Advanced Audiologist(Audiology) – Vestibular Focuspreferred


Band 7 – Suitable for newly qualifiedClinical Scientists


Full time, permanent


We’relooking for a Clinical Scientist/Advanced Audiologistwith a special interest in vestibular testing to join our friendly audiology team.


This is an exciting opportunity to join a service that provides care for adults and children, and the role offers the chance to practice other aspects of audiology alongside its vestibular focus.Wewould welcome applications from those who specialise inother aspects of Audiology as we have a variety of specialists within our team.We’realso happy to support applications for STP equivalencevia the Academy of Healthcare Science.


The roleis perfectly suited for candidates looking to develop theirleadershipskills. Itcomes with a variety of responsibilities related to quality assurance,supervisionand service development.






As an audiologist with a vestibular testing specialism,you’llbe responsible forvestibular assessment and rehabilitation in adults.You’llalso have theoptionto develop other clinical interests, including within our developing Bone Conduction Hearing Implant (BAHA) service.


The role may includeline management responsibilities and will offer opportunities to develop and lead on innovative projects within the team. As a senior clinician, the successful candidate will be supported to develop their leadership skills through further training and professional development.


The post-holder will have specialist knowledge of a wide range of procedures and practices underpinned by practical experience, and knowledgemaintainedthrough professional registration and CPD activity. To apply, youshouldhave NHS experience and a Masters-level qualification (or equivalent) in Audiology. Youmustalso have HCPC or RCCP registration to be considered for this role.


Ifyou’dlike to discuss this opportunity or arrange an informal visit with us, please contact Ann-Marie Hawkins or Shameela Munir on 024 7696 6444.


***The interview date for shortlisted applicants for this role is 18 June 2024. ****


University Hospitals Coventry and Warwickshire NHS Trust, rated as good by the Care Quality Commission, is one of the largest teaching Trusts in the UK.

We are extremely proud of our employees across our hospital sites, with high quality patient care at the heart of everything we do.

Boasting some of the most modern facilities in Western Europe, the Trust is renowned for being at the forefront of research and innovation as part of its blossoming reputation as a worldwide leader in healthcare.

We are proud to be recognised as a Pathway to Excellence®designated organisation – please click the link for further details about this prestigious award.Pathway To Excellence ® - University Hospitals Coventry & Warwickshire (uhcw.nhs.uk)

By joining our exciting journey, you will form part of a passionate, talented team and will be able to access a wide range of learning and development opportunities. There has never been a better time to join our team.

The Trust is committed to building an organisation that makes full use of the talents, skills, experience, and different perspectives available in our diverse society. We want everyone to feel they are respected, valued, can achieve their potential and receive the most appropriate and relevant care. We will create an environment where the equality and human rights principles of fairness, respect, equality, dignity and autonomy are promoted and are part of the organisation's core values.

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 IMP’s 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.


This advert closes on Monday 27 May 2024

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.

Cardinal Wiseman Catholic School

Teacher of Sports Science

MPS/UPS

Required from September 2024 - ECTs welcome to apply

We are seeking an inspirational Teacher of Sports Science to join us at Cardinal Wiseman Catholic School within The Romero Catholic Academy in Coventry.

This is an exciting time to be part of a growing team as we strive for academic excellence for all students in our care and we are looking for ambitious PGCE students or experienced teachers who are happy to specialise or teach through the range of ages.

We have recently been awarded "Good" in our last Ofsted Inspection and senior leaders have established an ambitious, knowledge-rich curriculum where students experience the very best knowledge in Sports Science.

Teachers receive high quality support and training to develop their practice and are well supported within the school to enable students to achieve their full potential.

If you are a passionate and motivated teacher who is focused on helping students develop a deep subject knowledge in order to achieve their true potential, we would welcome your application.

In return we can offer:
* a supportive leadership team and vibrant professional community
* quality training to those new to the career from our team of dedicated mentors
* a commitment to continuing professional development
* a positive school culture which believes in distributed and collaborative leadership
* energetic and enthusiastic highly motivated students
* a supportive, Catholic ethos across our school communities.

Visits to the school are welcomed and encouraged, please get in touch to arrange this.

For further details and an application form please contact Paul Hunt at Hays Education:
M: 07921583731
E:

We are committed to safeguarding and promoting the welfare of our students. All offers of employment will be subject to an enhanced DBS checks.

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

Cardinal Wiseman Catholic School

Teacher of Science

MPS/UPS (TLR negotiable for outstanding candidate)

Required from September 2024

"Cardinal Wiseman School is a happy place to be, where students behave well, achieve well and enjoy learning."
We are seeking an inspirational Teacher of Science to join Cardinal Wiseman Catholic School. This is an exciting time to be part of a growing team as we strive for academic excellence for all students in our care.

We have recently been awarded 'Good' in our last Ofsted Inspection and senior leaders have established an ambitious, knowledge-rich curriculum where students experience the very best knowledge in Science teaching.

This is an ideal opportunity for an ECT or an experienced teacher seeking a new challenge. Teachers receive high quality support and training to develop their practice and are well supported within the school to enable students to achieve their full potential. For a suitable candidate a TLR can be discussed based on skills and experience.

If you are a passionate and motivated teacher who is focused on helping students develop a deep subject knowledge in order to achieve their true potential, we would welcome your application.

In return we can offer:
* a supportive leadership team and vibrant professional community
* quality training to those new to the career from our team of dedicated mentors
* a commitment to continuing professional development
* a positive school culture which believes in distributed and collaborative leadership
* energetic and enthusiastic students
* a supportive, Catholic ethos across our school communities.

Visits to the school are welcomed and encouraged, please get in touch to arrange this.

For further details and an application form please contact Paul Hunt at Hays Education:
M: 07921583731
E:


We are committed to safeguarding and promoting the welfare of our students. All offers of employment will be subject to an enhanced DBS checks.

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 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.

The post holder will be responsible for the day to day management of several of the R&D clinical research studies and teams. The post holder will be supporting the safe conduct of research in accordance with the regulatory and legal frameworks relating to the planning, undertaking and closure of research studies providing assurance that the rights and well being of trial participants are protected.

Excellent support from the close-knit management team will be provided including a comprehensive induction package and the opportunity to really develop as a manager and leader of a patient focused, quality driven, cutting-edge service.

The post holder will be instrumental in implementing team objectives to enhance the performance and development of the research teams whilst providing guidance, education, leadership and co-ordinating the portfolio of research studies and clinical trials to deliver high quality research and clinical care.

The role integrates both clinical duties such as maintaining an active caseload and managerial duties; as such the post holder will be required to effectively manage their time to fulfil key responsibilities. It is also expected that the post holder will be flexible with hours of work as required to ensure that we are offering a service that best suits the needs of our patients.

The post holder will be employed by Research and Development department (R&D) to work within the central clinical research teams, managing an allocated number of research teams.

However, it is expected that the post folder will work flexibly across other research speciality areas as service requirements dictate throughout the duration of their contract.

The post holder will be responsible for the day to day management of several of the R&D clinical research studies and teams. The post holder will be supporting the safe conduct of research in accordance with the regulatory and legal frameworks relating to the planning, undertaking and closure of research studies providing assurance that the rights and well being of trial participants are protected.

The job holder may be required to carry out other similar or related duties within their bounds of registration which do not fall within the work outlined which may reasonably be required to deliver a comprehensive research service to our patients. The Line Manager, in consultation with the post holder will undertake any review.

University Hospitals Coventry and Warwickshire NHS Trust, rated as good by the Care Quality Commission, is one of the largest teaching Trusts in the UK.

We are extremely proud of our employees across our hospital sites, with high quality patient care at the heart of everything we do.

Boasting some of the most modern facilities in Western Europe, the Trust is renowned for being at the forefront of research and innovation as part of its blossoming reputation as a worldwide leader in healthcare.

We are proud to be recognised as a Pathway to Excellence®designated organisation – please click the link for further details about this prestigious award.Pathway To Excellence ® - University Hospitals Coventry & Warwickshire (uhcw.nhs.uk)

By joining our exciting journey, you will form part of a passionate, talented team and will be able to access a wide range of learning and development opportunities. There has never been a better time to join our team.

The Trust is committed to building an organisation that makes full use of the talents, skills, experience, and different perspectives available in our diverse society. We want everyone to feel they are respected, valued, can achieve their potential and receive the most appropriate and relevant care. We will create an environment where the equality and human rights principles of fairness, respect, equality, dignity and autonomy are promoted and are part of the organisation's core values.

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 patient’s 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 Health’s 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.


This advert closes on Monday 1 Apr 2024

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.

Barr's Hill School, Coventry

Lead Teacher of Science

MPS/UPS + TLR (negotiable depending on experience)

Required from September 2024

We are seeking to appoint an outstanding and motivated Lead teacher to join our strong Science team. As an outstanding classroom practitioner in all Key Stages the Lead Teacher will work with colleagues to improve and secure pupil outcomes, primarily via the development of the quality of teaching and learning through coaching and mentoring of colleagues and trainee teachers across the school. In addition, to play a major role supporting the leaders of teaching and learning in developing the strategic direction for T&L and to work with teachers across the school in collaborative planning, curriculum development and assessment, planning and moderation.


This is an exciting time to join Barr's Hill School and The Futures Trust. We are passionate about building brighter futures for our young people, and are driven by a set of compelling values:


1. Students First - students, staff, leaders, governors and trustees totally focused upon the educational benefit of our students within a safe and supportive environment
2. It's about learning - students, staff, leaders, governors and trustees totally focused upon developing and improving learning underpinned by harmonious and trusting relationships
3. No Barriers - no excuses, only support to ensure students, staff, leaders, governors and trustees maximise the academic achievement of students whilst enabling them to develop and flourish as well-rounded individuals


Barr's Hill is an 11-18 inner city school in the heart of Coventry. Our diverse student population is one of the many strengths of the school. We are looking for people who are ready to work with us on the next phase of our journey. Science is a thriving and popular subject, taught at all key stages, with students leaving us each year to top University courses.


Staff at Barr's Hill School are supported by experienced teachers, Middle and Senior Leaders who commit generously of their time to train and develop colleagues. The School offers focused CPD for all staff based on their future aspirations, and has a proven track record of developing excellent teachers and future leaders. The School fully funds Masters research and offers a range of outstanding leadership development opportunities, including collaboration across the Trust. ECT's are well supported by our induction programme which we lead regionally in partnership with the Futures Teaching Alliance and Best Practice.


Employees of the Trust have access to:
* Supported and funded professional development up to and including Masters level study
* Career pathways across the Trust
* The Teachers Pension Scheme
* Occupational Health Services
* 'Vivup' - employee benefits scheme offering discount at retail, travel, theme park and leisure providers
* Competitive rates of pay
* Family friendly policies


Informal visits to the school are very welcome and strongly encouraged, please get in touch if you would like to arrange this.


For more information, and to request an application pack, please contact Paul Hunt at Hays Education:
T: 07921583731
E:


Please also see our recruitment site: https://webmicrosites.hays.co.uk/web/barrs-hill-school


Barr's Hill School and The Futures Trust are committed to safeguarding and promoting the welfare of children and young people and require all staff and volunteers to share this commitment. The successful candidates for all positions will be subject to an enhanced DBS check and social media check.

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

This post would be suitable for a physiotherapist or other allied health professional with experience managing musculoskeletal disease especially with soft tissue knees.

The post will also develop research knowledge and skills and allow a research-interested allied health professional to progress their knowledge and skills in an exciting and world-famous team.

Please be advised that interviews are due to take place on 8th April.

The post holder will be responsible for the co-ordination of a defined group of clinical trials and research studies from set up to dissemination and archiving, meeting agreed patient recruitment targets and follow-up targets whilst coordinating and growing a research portfolio that has had many years of success. They will be patient-facing in their role and will engage in clinical activities as required by the post to contribute to this wider goal.

University Hospitals Coventry and Warwickshire NHS Trust, rated as good by the Care Quality Commission, is one of the largest teaching Trusts in the UK.

We are extremely proud of our employees across our hospital sites, with high quality patient care at the heart of everything we do.

Boasting some of the most modern facilities in Western Europe, the Trust is renowned for being at the forefront of research and innovation as part of its blossoming reputation as a worldwide leader in healthcare.

We are proud to be recognised as a Pathway to Excellence®designated organisation – please click the link for further details about this prestigious award.Pathway To Excellence ® - University Hospitals Coventry & Warwickshire (uhcw.nhs.uk)

By joining our exciting journey, you will form part of a passionate, talented team and will be able to access a wide range of learning and development opportunities. There has never been a better time to join our team.

The Trust is committed to building an organisation that makes full use of the talents, skills, experience, and different perspectives available in our diverse society. We want everyone to feel they are respected, valued, can achieve their potential and receive the most appropriate and relevant care. We will create an environment where the equality and human rights principles of fairness, respect, equality, dignity and autonomy are promoted and are part of the organisation's core values.
1. Facilitate the production of high-quality
2. Ensure that research is conducted within requirements of a multi-regulated clinical research
3. Provide a highly specialist, high standard clinical service, relevant to the needs of the post and qualifications of the successful applicant, assessing and advising the defined patient
4. Liaising with other appropriate clinical leads to ensure an integrated service is provided for the service area.
5. Provide support and advice for the continuous development, co-ordination and evaluation of the Knee Team pathways (therapy and trust pathways).
6. Provide a source of expert clinical opinion within the fields of knee surgery for therapy staff and/or other health care professionals both internal and particularly external to the Trust, appropriate to the specialist nature of procedures performed at UHCW NHS Trust.
7. Provide knowledge and expertise on the assessment and management of patients in this specialist service area
8. Raise the profile of the clinical research allied health professional role and the ongoing research in the team and wider trust.
9. Provide effective input into the work of the Trust, to support the achievement of our Trust

For further details please see the attached job description.


This advert closes on Thursday 21 Mar 2024