Total 36 science rd research job vacancies in ebbw vale blaenau gwent np23 4bx

DUTIES AND RESPONSIBILITIES The Education Manager will support the Workforce and Education Programme to: Plan and deliver educational initiatives for the multi-professional workforce, including developing eLearning modules, videos, webinars, and infographics, aligned with ACCEND. Identify key capabilities within ACCEND, ensuring all educational content aligns with national standards. Engage with Subject Matter Experts (SMEs) to establish a project steering group, incorporating input from research nurses, oncology experts, patient representatives, and the wider cancer workforce. Manage project timelines and deliverables, ensuring adherence to agreed schedules. Lead liaison with key stakeholders across the syste The indicative roles and responsibilities are as follows: Leadership and Expertise Commission the development of eLearning content, acting as the primary liaison between the Alliance and external developers. Lead the development of video scripts with subject matter experts in research, targeting common misconceptions about cancer research and clinical trials. Collaborate with communication and engagement to create infographics to boost understanding of various research and trial types, ensuring accessibility through consultations with the workforce. Collaborate with HEIs to incorporate cancer research into pre-registration curricula as part of the influencing curricula initiative. Develop a communication and engagement strategy in conjunction with the relevant teams to promote educational materials Set-Up and Organisation Lead a social media campaign focused on research and trials, promoting the educational toolkit. Launch webinars and promotional events, ensuring alignment with the broader Alliance education programme. Attend and contribute to research, workforce, and education meetings, aligning projects with broader programme ambitions Communication and Support Implement comprehensive communication skills training, aimed at enhancing patient advocacy and improving conversations about cancer research trials for the multidisciplinary workforce. Conduct a tender process for selecting a third-party developer to provide AI-based communication skills training. Collaborate with SMEs and the provider to develop communication scenarios that align with ACCEND capabilities, and create a marking scheme for assessment. Lead consultations on developed scenarios, gathering feedback to refine and validate the training material. Develop and distribute promotional materials to support the rollout of training programmes. Support discussions on developing a sustainable model for extending CCT access beyond research nurses. Collaborate with the Research Clinical Lead, Research Pathway Manager, and Senior Programme Lead to support project delivery and strategic alignment Data and Information Identify and engage clinical nurse specialists (CNSs) within the breast workforce for pilot testing communication training simulations. Establish baseline data for CNS participants, monitoring progress and outcomes throughout the pilot. Identify and track key metrics to measure the impact of educational activities on the workforce. Ensure that data is managed effectively and meets GDPR requirements Planning and Reporting Evaluate the workforce impact of the education provided, using data-driven insights to refine and improve offerings. Track and evaluate the effectiveness of CCT, including peer support meetings and evaluations of training initiatives like CanSurviveUK. Oversee budget management Lead sustainability initiatives, working with other cancer alliances and research organisations to promote and license the educational offerings for further use. Lead the definition of outcome measures that can be monitored during the year. Track progress against these outcome measures. Quality assure the programme against agreed standards and business plans, including for the timeliness and quality of reports and meeting of deadlines. Develop and maintain a risk register for the project, reporting risks and issues to the Senior Programme Lead for Education

We are looking for a highly motivated nurse, interested in helping to improve patient treatment outcomes for patients affected by lymphoma. Research nursing is an exciting and developing role, supported through the R&I division with a good education and development package in place to ensure that staff reach their potential.

This post presents an excellent opportunity to join the establishing and Lymphoma Research team with a varied portfolio of early and late clinical trials.

Central to this role is the responsibility of assessing and managing the care pathways including the delivery of all specified treatments for participants in research within a multidisciplinary team. Key responsibilities of the post include the co-ordination of the trial protocols and support for patient affected by lymphoma.

A background in oncology, flexibility in working, excellent communication and interpersonal skills are essential. Experience in clinical research and/or haematological malignancies would be desirable.

This advert is currently for a 12-month fixed contract as a maternity cover with a view to extend at the end of the post according to staffing at the time. This will be a band 5- 6 progression post. Competencies to be achieved for progression from band 5 to 6 will be focused on research delivery in oncology. This will include training sessions and work-based assessment.

As a Clinical Research Nurse (CRN), you will be providing patient-centred insights to the research delivery team by supporting both the patients and the team through all aspects of clinical research of the Lymphoma portfolio.

You will be involved in every stage of the portfolio activities including feasibility reviews and set-up of and new trials. Patient recruitment and management is a key part of the role, including the administration of complex treatment regimes. You will be supporting team with data query resolution and reviewing protocol amendments.

You will be required to have excellent communication and interpersonal skills, possess strong motivation and have the ability to work independently.

With support from the team the CRN will ensure that the safety and wellbeing of the patients is maintained within the requirement of the multi-regulatory frameworks for clinical research ensuring compliance with ICH/GCP standards and Trust SOPs.

You will be able to raise the profile of the clinical research nurse and clinical trials within the trust by engaging in promotional events relating to clinical research with attendance and contributions at local, national and international meetings. As part of the role, you will need to demonstrate awareness and contribution to divisional, Trust and national objectives and strategies.

The Christie NHS Foundation Trust is one of the leading cancer centres in Europe, offering high quality diagnosis, treatment and care as well as being at the forefront of cancer research and education.



As a key member of the Lymphoma Research Team, you join a dynamic and supportive team at the forefront of haematology research and centred around patient treatment and care. Working with a team of Research Nurses, Clinical Trials Coordinators and Investigators you will support the delivery of commercial, non-commercial and academic trials. We put emphasis on individual’s and team’s development and encourage engagement from all team members into meetings and system improvement projects. An exposure to a variety of trials, tasks and processes enables professional and continuous growth.

DUTIES AND RESPONSIBILITIES



Clinical Research Co-ordination


• Work autonomously in all areas of practice relating to clinical research.
• Understand and deliver care in accordance with regulatory approved clinical research protocols.
• Understand the process for obtaining NHS permissions (R&D approval) for conducting clinical trials at site. As project lead, ensure permissions are in place prior to any patient recruitment.
• Participate in clinical trial feasibilities and risk assessments of clinical trial protocols.
• Ensure all clinical trial activities are recorded in appropriate systems in a timely manner.
• Awareness of trial specific, regional and national targets. Identify and implement strategies for recruiting patients to clinical trials ensuring that targets for patient recruitment are delivered.
• Delegation and oversight of research related activities to research team members (clinical and administrative) and ensure compliance with SOPs and ICH/GCP
• Arrange and facilitate clinical trial related meetings.
• Involvement in appropriate financial remunerations for clinical trial activity.



Clinical Service and Professional Responsibilities


• Assimilation of highly complex information relating to clinical trials and communication to patients at a level appropriate to their understanding. Ensure highly sensitive information is communicated to patients, relatives and carers regarding prognosis
• Contribute to the development, implementation and review of specialist care pathways in conjunction with appropriate personnel.
• Demonstration of expert knowledge in specialist area to maintain clinical excellence.
• Demonstrate awareness of divisional and trust strategic objectives including performance indicators and metrics.
• Escalation of governance issues impacting on delivery of job purpose.
• To act as a primary contact point for the clinical trial patients and act as adviser to other health care professionals.
• Responsibility for maintenance and development of professional knowledge and practice by attending mandatory and specialist training in accordance with local policy
• Ensuring care delivery standards in accordance with trial protocol, local policy, NMC Code of Practice Conduct and current best practice.
• Development and maintenance of a high quality service by:
• Overseeing the safe administration of all licensed and unlicensed medicinal products within the context of a clinical trial.
• Overseeing assessment and evaluation of treatment toxicities and initiation of appropriate intervention.
• Contribute to development of specialist Standard Operating Procedures and guidelines
• Provide education and support for non-research staff in the delivery of protocol driven treatment for all patients.
• Participate in monitoring and audit activities within research team
• To carry out non-medical prescribing within scope of professional practice and in accordance with local policies and procedures and national legislation (optional and depending on clinical service needs)



Personal Education, Training and Development


• Maintain professional development whilst evaluating own specialist knowledge and practice through a process of appraisal and personal development planning.
• Promote the role of the clinical research nurse as an integral part of the healthcare system.
• Increase and maintain awareness of current advances in cancer treatments, research and nursing practice thereby maintaining the highest standard of care for patients with cancer and implementing evidence based care by continuing professional development.
• Participation in trust-wide education programmes and study days.
• Obtain clinical supervision as appropriate.
• To keep up to date with departmental, Trust, UK and EU developments for the management of clinical research ensuring timely, effective implementation of changes.
• Attendance at team and divisional meeting Staff Management and Development
• To Support the Senior Clinical Research Nurse in the induction and continued supervision of junior members of staff, ensuring compliance with regulatory compliance and legislation.
• Support the development of specialist study days within own research team.
• Assist in the provision of specialist education and training in relation to clinical trials to all key stakeholders.
• Disseminate information by attendance and /or presentations at local, national and international conferences/meetings
• Contribute to the development of members of the research tea
• EU DIRECTIVE ICH/GCP All personnel involved in clinical research have a responsibility to ensure that clinical trials are conducted in accordance with the EU Directive and ICH/GCP.


This advert closes on Tuesday 19 Nov 2024

Proud member of the Disability Confident employer scheme

ORGANISATIONAL ARRANGEMENTSThis post is for a 12-month fixed term contract for a clinical Fellow to join the Medical Oncologymelanoma service for 40 hours per week.This post is for 40 hours per week Role PurposeThis is a 10 session SpR equivalent Trust Grade post. It is based at the Christie site in the departmentof Medical Oncology. This position is suitable for individuals who wish to gain specialist training andexperience in the care of patients with melanoma, and further training in early phase clinical trials.The Melanoma Team is a multi-disciplinary team of surgeons, oncologists and research staff. Thereare 4 plastic surgeons, 2 clinical oncologists, 4 medical oncologists and a large clinical research team.The oncology team covers a population of > 3.5 million and sees approximately 2250 new patients ayear with high risk primary or advanced disease. The team is a major contributor to clinical researchat a national and international level. We work closely with colleagues in the CRUK ManchesterInstitute, one of 3 CRUK Super Centres in the UK, and with colleagues at the University ofManchester (, Dr Adam Hurlstone). Manchester Cancer Research Centre has prioritised melanomaas one of six areas in which it will be internationally leading in research.The post will offer experience in cutting edge research in personalised medicine andimmunotherapy, Early Phase trials methodology and conduct, and experience in managing complexcases in an academic tertiary care centre with an international reputation. In addition, there areongoing projects inn toxicity management, late effects and on the use of big data and interrogationof national data-sets. It is expected the successful applicant will publish a number of papers as aresult of their attachment, and there will be an opportunity to develop novel research projects. The role will be responsible for: DUTIES AND RESPONSIBILITIES 1. Main Duties: To work as a Clinical Fellow at the Christie under the supervision of Professor Paul Lorigan, Dr Avinash Gupta, Dr Patricio Serra and Dr Rebecca Lee. This will involve close liaison with other members of the multidisciplinary team in particular surgeons, research nurses and data managers. A major role of the post will be to implement evidence based best practice for patients who are being treated on clinical trials at the Christie and to develop and support associated clinical research.2. Clinical Management: to work closely with and support the team in the management of patients with melanoma. An important role of the Clinical Fellow will be to have direct involvement in the day-to-day clinical management of patients under the supervision of the consultant whether or not they are being managed within the confines of a clinical trial, and to attend relevant MDTs, radiology and educational meetings. 3. Clinics: the Clinical Fellow will be required to support research and NHS clinics, typically 4clinics per week: examples - Monday am (treatment and research), Monday pm (new andfollow-up), Wednesday pm (new, FU and treatments), Thursday (new). .4. Protocols: the post holder will be expected to revise and develop evidence based protocolsfor patients. He/she will be expected to undertake the administrative duties associated withthe care of these patients.5. Professional Development: He/she will maintain a level of continuing professionaldevelopment consistent with the recommendations of the Royal College of Physicians.Appropriate arrangements for study leave will be made in conjunction with colleagues. Afund, administered by the Director of Service for the support of study leave exists within theTrust. The post holder will also be required to undergo an appraisal.6. Junior Doctor Training: the post holder will be expected to contribute actively to the trainingof ST1 & 2s in medical oncology and of medical students form the University of ManchesterThe post holder will also be expected to help in the training of nursing and multidisciplinarystaff in both inpatient and outpatient departments.7. Clinical Governance: the post holder will be expected to participate in all relevant aspects ofclinical governance, including maintaining up to date protocols, guidelines and clinical audit,under the supervision of the other consultants in the unit.8. Audit: the appointee will play a full role in clinical audit as a member of the Christie HospitalMedical Staff.9. Research: there are excellent opportunities for research within the department. Theappointee will be encouraged to contribute to current research projects within the unitand/or set up new projects in consultation with supervisors. Successful candidates will beencouraged to submit research findings for presentation at national or internationalmeetings and will be supported to attend these. On call: the post does not attract an on-call commitment. Continuing Professional DevelopmentThe Trust supports the requirements for continuing professional development (CPD) as laid down by the GMC and surgical colleges and is committed to providing time and financial support for these activities. Role Planning Provisional Sessional Timetable for Clinical Fellow in Medical Oncology Proposed Sessional Activities:CLINICALOutpatients Clinic 4Ward Rounds 1MDT 0.25Clinical meeting/Morbitidy and mortality meeting 0.5Support of research nurses/data managers 1-2Personal research and CPD 3-4 A sessional activity is 4 hours Monday Tuesday Wednesday Thursday Friday AM Research clinic Educational meeting (once a month) Personal Research &CPDSupport for researchnurses/data managers Ward round Supportresearch staff Personal research &CPDSupport for researchnurses/datamanagersWeekly researchmeeting Personal research& CPD PM Clinic Research clinicSpecialist meeting(once a month) Clinic MDT alternate weeks Clinic Personal research& CPDSupport researchstaff On call CommitmentsThis role does not require participation in the on-call rota.

Please note that this post is offered as a permanent contract at 37.5 h/week.

An exciting opportunity has arisen within the Research and Innovation Division at The Christie. We are looking to appoint a Senior Clinical Research Nurse to the Lung research delivery team within The Christie NHS Foundation Trust.

This post presents an opportunity to join an established research team with a varied portfolio of clinical trials as a Senior Clinical Research Nurse (sCRN). The Lung cancer research team is responsible for a varied portfolio of academic and commercial clinical trials.

Key responsibilities of the post include supporting the coordination of the patient’s pathway through an agreed portfolio of clinical trials across Lung. Excellent communications skills in all forms are required for this role for difficult clinical conversations with patients and their families. Experience of line management and excellent leadership skills are required.

The successful candidate will be someone with excellent organisational, time management, leadership skills to be the key contact for patients and wider MDT who are being considered for Lung clinical trials.

Central to this role is the responsibility of assessing and managing the complex needs of patients participating in a clinical trial.

Management of staff and evidence of service improvement are vital

Experience in oncology and research is essential.

This position involves leading and managing a group of research nurses while supporting the Research Nurse Team Leader. Ensuring that research is conducted within the requirements of a multiregulated clinical research environment and safeguarding patient wellbeing are key responsibilities. Excellent communication and interpersonal skills are essential, in line with The Christie values. The role requires a strong motivation and the ability to work independently. A background in oncology and research is essential, along with experience in leadership and flexibility in working.

The sCRN will interact with a variety of research professionals across The Christie, including the NIHR Manchester Clinical Research Facility, as well as across Manchester and wider networks. A proactive approach to self-development and the ability to demonstrate initiative and expertise in team development and wider training programmes are important. By utilising national frameworks for auditing patient experiences, the sCRN will ensure that patients in the Lung disease portfolio studies have the best possible experience while participating in clinical research.

Additionally, the role involves raising the profile of the clinical research nurse and clinical trials within the trust by engaging in promotional events related to clinical research and contributing at local, national, and international meetings.

The Lung disease team consists of nurses and consultants with clinical trial coordination and project management support. The portfolio is driven to deliver treatment opportunities to as many patients with Lung at The Christie as possible.

There is a close working relationship with all members of the team with a strategy to increase recruitment into these niche protocols thus offering patients more opportunities to be involved in clinical research. We are looking for a dynamic, highly motivated individual to join our team, to help develop streamlined ways of cross-team working and to provide our research patients with the best possible experience.

The team is highly collaborative in its working practices in order to promote the teams achievements throughout the R&I division, NIHR and with our commercial sponsors with regular reviews of performance & clinical trial feasibilities and service improvement to ensure the highest possible experience for the team and our patients and their families.

DUTIES AND RESPONSIBILITIES



Clinical Research Co-ordination
• Work autonomously in all areas of practice relating to clinical research.
• Understand and deliver care in accordance with regulatory approved clinical research protocols.
• Oversee the process for obtaining NHS permissions (R&D approval) for clinical trials within team. As project lead, ensures permissions are in place prior to any patient recruitment.
• Undertake feasibility and risk assessments of clinical trial protocols in conjunction with Team Leader, Principal Investigator and Senior Clinical Trials Co-Ordinator
• Ensure all clinical trial activities are recorded in appropriate systems in a timely manner.
• Awareness of trial specific, regional, and national targets.
• Initiate new recruitment strategies for recruiting patients to clinical trials including engagement with the research network.
• In conjunction with Team Leader lead on the delegation of all trial related activities to research team members (clinical and administrative) and ensure compliance with SOPs and ICH/GCP.
• Work with team leader and sponsor companies in the preparation and negotiation of financial contracts for individual trials.
• Arrange and facilitate clinical trial related meetings.
• In conjunction with Team Leader, oversee appropriate financial remunerations for clinical trial activity



Clinical Service and Professional Responsibilities
• Assimilation of highly complex information relating to clinical trials and communication to patients at a level appropriate to their understanding. Ensure highly sensitive information is communicated to patients, relatives, and careers regarding prognosis
• Responsible for the development, implementation, and review of specialist care pathways in conjunction with appropriate personnel.
• Demonstration of expert knowledge in specialist area to maintain clinical excellence.
• Set up processes/patient pathways in conjunction with appropriate personnel from specialist research areas to promote a cost-effective timely service for individual protocols (shared care pathways, specialist clinics, etc.).
• Support Team Leader in delivering divisional and trust strategic objectives including performance indicators and metrics.
• Escalation of governance issues impacting on delivery of job purpose.
• To act as a primary contact point for the clinical trial patients and act as adviser to other health care professionals.
• Responsibility for maintenance and development of professional knowledge and practice by attending mandatory and specialist training (e.g., GCP) in accordance with local policy
• Ensuring care delivery standards in accordance with trial protocol, local policy, NMC Code of Practice Conduct and current best practice
• Development and maintenance of a high-quality service by:
1. Overseeing the safe administration of all licensed and unlicensed medicinal products within the context of a clinical trial.
2. Overseeing assessment and evaluation of treatment toxicities and initiation of appropriate intervention.
3. Contribute to development of specialist Standard Operating Procedures and guidelines
• Provide education and support for non-research staff in the delivery of protocol driven treatment for all patients.
• Participate in monitoring and audit activities within research team
• To carry out non-medical prescribing within scope of professional practice and in accordance with local policies and procedures and national legislation (optional and depending on clinical service needs).



Personal Education, Training and Development
• Maintain professional development whilst evaluating own specialist knowledge and practice through a process of appraisal and personal development planning.
• Promote the role of the clinical research nurse as an integral part of the healthcare system.
• Increase and maintain awareness of current advances in cancer treatments, research and nursing practice thereby maintaining the highest standard of care for patients with cancer and implementing evidence-based care by continuing professional development.
• Participation in trust-wide education programs and study days.
• Obtain clinical supervision as appropriate.
• To keep up to date with departmental, Trust, UK and EU developments for the management of clinical research ensuring timely, effective implementation of changes.
• Attendance at team and divisional meetings



Staff Management and Development
• In conjunction with the team leader, provide the induction, continued supervision and management of the research teams.
• In conjunction with the team leader, be responsible for ensuring all members of the research nurse team undergo regular appraisal and support appropriate training and development opportunities in line with role requirements.
• Lead on the development of specialist study days within own research team
• Provide specialist education and training in relation to clinical trials to all key stakeholders.
• Disseminate information by attendance and /or presentations at local, national and international conferences/meetings
• Be responsible for the development of members of the research team.



EU DIRECTIVE ICH/GCP
• All personnel involved in clinical research have a responsibility to ensure that clinical trials are conducted in accordance with the EU Directive and ICH/GCP.


This advert closes on Wednesday 6 Nov 2024

Proud member of the Disability Confident employer scheme

An exciting opportunity has arisen within the Research and Innovation Division. We are looking to appoint a Clinical Research Fellow to the Melanoma research team. This post presents an opportunity to join an established research team with a varied portfolio of clinical trials as a Clinical Research Fellow. The Melanoma disease research team is responsible for a varied portfolio of academic and commercial clinical trials. It is based at the Christie site in the department of Medical Oncology. This position is suitable for individuals who wish to gain specialist training and experience in the care of patients with melanoma, and further training in early phase clinical trials. The Melanoma Team is a multi-disciplinary team of surgeons, oncologists and research staff. The team is a major contributor to clinical and translational research. The post will offer experience in cutting edge research in personalised medicine and immunotherapy, Early Phase trials, and experience in managing complex cases in an academic tertiary care centre with an international reputation. In addition, there are ongoing projects in toxicity management, late effects and on the use of big data and interrogation of national data-sets. It is expected the successful applicant will publish a number of papers as a result of their attachment, and there will be an opportunity to develop novel research projects.

To work as a Clinical Research Fellow at the Christie under the supervision of Professor Paul Lorigan, Dr Avinash Gupta, Dr Patricio Serra and Dr Rebecca Lee. This will involve close liaison with other members of the multidisciplinary team in particular surgeons, research nurses and data managers. A major role of the post will be to implement evidence based best practice for patients who are being treated on clinical trials at the Christie and to develop and support associated clinical research.
to work closely with and support the team in the management of patients with melanoma. An important role of the Clinical Fellow will be to have direct involvement in the day-to-day clinical management of patients under the supervision of the consultant whether or not they are being managed within the confines of a clinical trial, and to attend relevant MDTs, radiology and educational meetings.
The Clinical Fellow will be required to support research and NHS clinics, typically 4 clinics per week
The post does not attract an on-call commitment.

The Christie is one of Europe’s leading cancer centres, treating over 60,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 15% patients are referred to us from other parts of the country.
The Melanoma disease team is a small team of nurses and consultants with clinical trial coordination and project management support. The portfolio is driven to deliver treatment opportunities to as many patients with Melanoma at The Christie as possible.
There is a close working relationship with all members of the team with a strategy to increase recruitment into these niche protocols thus offering patients more opportunities to be involved in clinical research. We are looking for a dynamic, highly motivated individual to join our team, to help develop streamlined ways of cross-team working and to provide our research patients with the best possible experience.
The team is highly collaborative in its working practices in order to promote the teams achievements throughout the R&I division, NIHR and with our commercial sponsors with regular reviews of performance & clinical trial feasibilities and service improvement to ensure the highest possible experience for the team and our patients and their families.

ORGANISATIONAL ARRANGEMENTS
This post is for a 12-month fixed term contract for a clinical Fellow to join the Medical Oncology
melanoma service for 40 hours per week.
This post is for 40 hours per week

Role Purpose
This is a 10 session SpR equivalent Trust Grade post. It is based at the Christie site in the department
of Medical Oncology. This position is suitable for individuals who wish to gain specialist training and
experience in the care of patients with melanoma, and further training in early phase clinical trials.
The Melanoma Team is a multi-disciplinary team of surgeons, oncologists and research staff. There
are 4 plastic surgeons, 2 clinical oncologists, 4 medical oncologists and a large clinical research team.
The oncology team covers a population of > 3.5 million and sees approximately 2250 new patients a
year with high risk primary or advanced disease. The team is a major contributor to clinical research
at a national and international level. We work closely with colleagues in the CRUK Manchester
Institute, one of 3 CRUK Super Centres in the UK, and with colleagues at the University of
Manchester (, Dr Adam Hurlstone). Manchester Cancer Research Centre has prioritised melanoma
as one of six areas in which it will be internationally leading in research.
The post will offer experience in cutting edge research in personalised medicine and
immunotherapy, Early Phase trials methodology and conduct, and experience in managing complex
cases in an academic tertiary care centre with an international reputation. In addition, there are
ongoing projects inn toxicity management, late effects and on the use of big data and interrogation
of national data-sets. It is expected the successful applicant will publish a number of papers as a
result of their attachment, and there will be an opportunity to develop novel research projects.


The role will be responsible for:

DUTIES AND RESPONSIBILITIES

1. Main Duties: To work as a Clinical Fellow at the Christie under the supervision of Professor Paul Lorigan, Dr Avinash Gupta, Dr Patricio Serra and Dr Rebecca Lee. This will involve close liaison with other members of the multidisciplinary team in particular surgeons, research nurses and data managers. A major role of the post will be to implement evidence based best practice for patients who are being treated on clinical trials at the Christie and to develop and support associated clinical research.
2. Clinical Management: to work closely with and support the team in the management of patients with melanoma. An important role of the Clinical Fellow will be to have direct involvement in the day-to-day clinical management of patients under the supervision of the consultant whether or not they are being managed within the confines of a clinical trial, and to attend relevant MDTs, radiology and educational meetings.


3. Clinics: the Clinical Fellow will be required to support research and NHS clinics, typically 4
clinics per week: examples - Monday am (treatment and research), Monday pm (new and
follow-up), Wednesday pm (new, FU and treatments), Thursday (new). .
4. Protocols: the post holder will be expected to revise and develop evidence based protocols
for patients. He/she will be expected to undertake the administrative duties associated with
the care of these patients.
5. Professional Development: He/she will maintain a level of continuing professional
development consistent with the recommendations of the Royal College of Physicians.
Appropriate arrangements for study leave will be made in conjunction with colleagues. A
fund, administered by the Director of Service for the support of study leave exists within the
Trust. The post holder will also be required to undergo an appraisal.
6. Junior Doctor Training: the post holder will be expected to contribute actively to the training
of ST1 & 2s in medical oncology and of medical students form the University of Manchester
The post holder will also be expected to help in the training of nursing and multidisciplinary
staff in both inpatient and outpatient departments.
7. Clinical Governance: the post holder will be expected to participate in all relevant aspects of
clinical governance, including maintaining up to date protocols, guidelines and clinical audit,
under the supervision of the other consultants in the unit.
8. Audit: the appointee will play a full role in clinical audit as a member of the Christie Hospital
Medical Staff.
9. Research: there are excellent opportunities for research within the department. The
appointee will be encouraged to contribute to current research projects within the unit
and/or set up new projects in consultation with supervisors. Successful candidates will be
encouraged to submit research findings for presentation at national or international
meetings and will be supported to attend these.

On call: the post does not attract an on-call commitment.

Continuing Professional Development
The Trust supports the requirements for continuing professional development (CPD) as laid down by the GMC and surgical colleges and is committed to providing time and financial support for these activities.

Role Planning

Provisional Sessional Timetable for Clinical Fellow in Medical Oncology

Proposed Sessional Activities:
CLINICAL
Outpatients Clinic 4
Ward Rounds 1
MDT 0.25
Clinical meeting/Morbitidy and mortality meeting 0.5
Support of research nurses/data managers 1-2
Personal research and CPD 3-4


A sessional activity is 4 hours



Monday

Tuesday

Wednesday

Thursday

Friday

AM

Research clinic

Educational meeting (once a month) Personal Research &
CPD
Support for research
nurses/data managers

Ward round Support
research staff

Personal research &
CPD
Support for research
nurses/data
managers
Weekly research
meeting

Personal research
& CPD

PM

Clinic

Research clinic
Specialist meeting
(once a month)

Clinic

MDT alternate weeks Clinic

Personal research
& CPD
Support research
staff





On call Commitments
This role does not require participation in the on-call rota.


This advert closes on Monday 4 Nov 2024

Proud member of the Disability Confident employer scheme

DUTIES AND RESPONSIBILITIES: Clinical Research Co-ordination Work autonomously in all areas of practice relating to clinical research. Understand and deliver care in accordance with regulatory approved clinical research protocols. Understand the process for obtaining NHS permissions (R&D approval) for conducting clinical trials at site. As project lead, ensure permissions are in place prior to any patient recruitment. Participate in clinical trial feasibilities and risk assessments of clinical trial protocols. Ensure all clinical trial activities are recorded in appropriate systems in a timely manner. Awareness of trial specific, regional and national targets. Identify and implement strategies for recruiting patients to clinical trials ensuring that targets for patient recruitment are delivered. Delegation and oversight of research related activities to research team members (clinical and administrative) and ensure compliance with SOPs and ICH/GCP. Arrange and facilitate clinical trial related meetings. Involvement in appropriate financial remunerations for clinical trial activity. Clinical Service and Professional Responsibilities Assimilation of highly complex information relating to clinical trials and communication to patients at a level appropriate to their understanding. Ensure highly sensitive information is communicated to patients, relatives, and carers regarding prognosis Contribute to the development, implementation, and review of specialist care pathways in conjunction with appropriate personnel. Demonstration of expert knowledge in specialist area to maintain clinical excellence. Demonstrate awareness of divisional and trust strategic objectives including performance indicators and metrics. Escalation of governance issues impacting on delivery of job purpose. To act as a primary contact point for the clinical trial patients and act as adviser to other health care professionals. Responsibility for maintenance and development of professional knowledge and practice by attending mandatory and specialist training in accordance with local policy. Ensuring care delivery standards in accordance with trial protocol, local policy, NMC Code of Practice Conduct and current best practice. Development and maintenance of a high-quality service by: Overseeing the safe administration of all licensed and unlicensed medicinal products within the context of a clinical trial. Overseeing assessment and evaluation of treatment toxicities and initiation of appropriate intervention. Contribute to development of specialist Standard Operating Procedures and guidelines. Provide education and support for non-research staff in the delivery of protocol driven treatment for all patients. Participate in monitoring and audit activities within research team To carry out non-medical prescribing within scope of professional practice and in accordance with local policies and procedures and national legislation (optional and depending on clinical service needs). Personal Education, Training and Development Maintain professional development whilst evaluating own specialist knowledge and practice through a process of appraisal and personal development planning. Promote the role of the clinical research nurse as an integral part of the healthcare system. Increase and maintain awareness of current advances in cancer treatments, research and nursing practice thereby maintaining the highest standard of care for patients with cancer and implementing evidence-based care by continuing professional development. Participation in trust-wide education programmes and study days. Obtain clinical supervision as appropriate. To keep up to date with departmental, Trust, UK and EU developments for the management of clinical research ensuring timely, effective implementation of changes. Attendance at team and divisional meeting Staff Management and Development To Support the Senior Clinical Research Nurse in the induction and continued supervision of junior members of staff, ensuring compliance with regulatory compliance and legislation. Support the development of specialist study days within own research team. Assist in the provision of specialist education and training in relation to clinical trials to all key stakeholders. Disseminate information by attendance and /or presentations at local, national and international conferences/meetings Contribute to the development of members of the research team EU DIRECTIVE ICH/GCP All personnel involved in clinical research have a responsibility to ensure that clinical trials are conducted in accordance with the EU Directive and ICH/GCP.

We are looking to appoint a Clinical Research Nurse (Band 6) in the Renal and Oesophagogastric Research team within The Christie NHS Foundation Trust. The successful candidate will have either oncology or research experience.

The successful candidate will be working with an established research team with a large and varied portfolio of phase I to phase III studies. The post holder will care for patients with gastric or oesophageal cancer who are receiving systemic anti-cancer treatments and/or radiotherapy within a clinical trial and work alongside a team of consultants, clinical fellows, clinical research nurses and clinical trial administrators.

While we are looking to recruit a full-time (37.5 hours/ 5days) Clinical Research Nurse to support our busy team, we would consider applicants wanting part-time hours.

An informal conversation to discuss the post is highly recommended.

As a Clinical Research Nurse working within the Renal and Oesophagogastric team, you will be the lead research nurse of your own portfolio of clinical trials as well as acting as the key point of contact for patients. Your day-to-day role will include supporting clinical trial recruitment, co-ordination of care and organisation of treatment, supporting patients while they receive treatment within a clinical trial, acting as key point of contact for clinical trial sponsors and clinical research organisations and data entry.

You will work closely with and be supported by the Senior Clinical Research Nurse as well as the other Clinical Research Nurses on the team. You will be provided with a comprehensive training and supernumerary period to support your learning for this role.

The Renal and Oesophagogastric team works on studies including early phase, biomarker trials, real-world data, IMP trials, radiotherapy trials and will eventually be involved in innovative proton beam trials. The Christie’s research teams contribute towards pioneering research and innovation and we constantly work towards improving cancer care and patient outcomes.

The Christie NHS Foundation Trust is one of the largest cancer treatment centres in Europe, and an international leader in cancer research and development. We are one of the leading centres in the UK for clinical trials and radiotherapy research. Treating more than 60,000 patients a year, we are the first UK centre to be officially accredited as a comprehensive cancer centre. The Clinical Research Facility (CRF) at The Christie is also one of four specialist units in Manchester for experimental research that make up the NIHR Manchester CRF, providing us with the dedicated space and expertise required to deliver intensive and complex studies in safe environment.

In December 2018 The Christie became home to one of only two high energy NHS proton beam therapy (PBT) centres in the UK where we provide specialised treatment for UK patients with complex and hard-to-treat cancers who would otherwise be required to have this treatment abroad at centres in either Europe or in the USA.

We are ranked as the most technologically advanced cancer centre in the world outside North America, and have been named, by the National Institute for Health Research, as one of the best hospitals providing opportunities for patients to take part in clinical research studies.

DUTIES AND RESPONSIBILITIES:

Clinical Research Co-ordination

· Work autonomously in all areas of practice relating to clinical research.

· Understand and deliver care in accordance with regulatory approved clinical research protocols.

· Understand the process for obtaining NHS permissions (R&D approval) for conducting clinical trials at site. As project lead, ensure permissions are in place prior to any patient recruitment.

· Participate in clinical trial feasibilities and risk assessments of clinical trial protocols.

· Ensure all clinical trial activities are recorded in appropriate systems in a timely manner.

· Awareness of trial specific, regional and national targets. Identify and implement strategies for recruiting patients to clinical trials ensuring that targets for patient recruitment are delivered.

· Delegation and oversight of research related activities to research team members (clinical and administrative) and ensure compliance with SOPs and ICH/GCP.

· Arrange and facilitate clinical trial related meetings.

· Involvement in appropriate financial remunerations for clinical trial activity.



Clinical Service and Professional Responsibilities

· Assimilation of highly complex information relating to clinical trials and communication to patients at a level appropriate to their understanding. Ensure highly sensitive information is communicated to patients, relatives, and carers regarding prognosis

· Contribute to the development, implementation, and review of specialist care pathways in conjunction with appropriate personnel.

· Demonstration of expert knowledge in specialist area to maintain clinical excellence.

· Demonstrate awareness of divisional and trust strategic objectives including performance indicators and metrics.

· Escalation of governance issues impacting on delivery of job purpose.

· To act as a primary contact point for the clinical trial patients and act as adviser to other health care professionals.

· Responsibility for maintenance and development of professional knowledge and practice by attending mandatory and specialist training in accordance with local policy.

· Ensuring care delivery standards in accordance with trial protocol, local policy, NMC Code of Practice Conduct and current best practice.

· Development and maintenance of a high-quality service by:

Ø Overseeing the safe administration of all licensed and unlicensed medicinal products within the context of a clinical trial.

Ø Overseeing assessment and evaluation of treatment toxicities and initiation of appropriate intervention.

Ø Contribute to development of specialist Standard Operating Procedures and guidelines.

· Provide education and support for non-research staff in the delivery of protocol driven treatment for all patients.

· Participate in monitoring and audit activities within research team

· To carry out non-medical prescribing within scope of professional practice and in accordance with local policies and procedures and national legislation (optional and depending on clinical service needs).



Personal Education, Training and Development

· Maintain professional development whilst evaluating own specialist knowledge and practice through a process of appraisal and personal development planning.

· Promote the role of the clinical research nurse as an integral part of the healthcare system.

· Increase and maintain awareness of current advances in cancer treatments, research and nursing practice thereby maintaining the highest standard of care for patients with cancer and implementing evidence-based care by continuing professional development.

· Participation in trust-wide education programmes and study days.

· Obtain clinical supervision as appropriate.

· To keep up to date with departmental, Trust, UK and EU developments for the management of clinical research ensuring timely, effective implementation of changes.

· Attendance at team and divisional meeting



Staff Management and Development

· To Support the Senior Clinical Research Nurse in the induction and continued supervision of junior members of staff, ensuring compliance with regulatory compliance and legislation.

· Support the development of specialist study days within own research team.

· Assist in the provision of specialist education and training in relation to clinical trials to all key stakeholders.

· Disseminate information by attendance and /or presentations at local, national and international conferences/meetings

· Contribute to the development of members of the research team

_______________________________________________________________

EU DIRECTIVE ICH/GCP

All personnel involved in clinical research have a responsibility to ensure that clinical trials are conducted in accordance with the EU Directive and ICH/GCP.


This advert closes on Wednesday 2 Oct 2024

Proud member of the Disability Confident employer scheme

DUTIES AND RESPONSIBILITIES Clinical Research Co-ordination Work autonomously in all areas of practice relating to clinical research. Understand and deliver care in accordance with regulatory approved clinical research protocols. Oversee the process for obtaining NHS permissions (R&D approval) for clinical trials within team. As project lead, ensures permissions are in place prior to any patient recruitment. Undertake feasibility and risk assessments of clinical trial protocols in conjunction with Team Leader, Principal Investigator and Senior Clinical Trials Co-Ordinator Ensure all clinical trial activities are recorded in appropriate systems in a timely manner. Awareness of trial specific, regional, and national targets. Initiate new recruitment strategies for recruiting patients to clinical trials including engagement with the research network. In conjunction with Team Leader lead on the delegation of all trial related activities to research team members (clinical and administrative) and ensure compliance with SOPs and ICH/GCP. Work with team leader and sponsor companies in the preparation and negotiation of financial contracts for individual trials. Arrange and facilitate clinical trial related meetings. In conjunction with Team Leader, oversee appropriate financial remunerations for clinical trial activity Clinical Service and Professional Responsibilities Assimilation of highly complex information relating to clinical trials and communication to patients at a level appropriate to their understanding. Ensure highly sensitive information is communicated to patients, relatives, and careers regarding prognosis Responsible for the development, implementation, and review of specialist care pathways in conjunction with appropriate personnel. Demonstration of expert knowledge in specialist area to maintain clinical excellence. Set up processes/patient pathways in conjunction with appropriate personnel from specialist research areas to promote a cost-effective timely service for individual protocols (shared care pathways, specialist clinics, etc.). Support Team Leader in delivering divisional and trust strategic objectives including performance indicators and metrics. Escalation of governance issues impacting on delivery of job purpose. To act as a primary contact point for the clinical trial patients and act as adviser to other health care professionals. Responsibility for maintenance and development of professional knowledge and practice by attending mandatory and specialist training (e.g., GCP) in accordance with local policy Ensuring care delivery standards in accordance with trial protocol, local policy, NMC Code of Practice Conduct and current best practice Development and maintenance of a high-quality service by: o Overseeing the safe administration of all licensed and unlicensed medicinal products within the context of a clinical trial. o Overseeing assessment and evaluation of treatment toxicities and initiation of appropriate intervention. o Contribute to development of specialist Standard Operating Procedures and guidelines Provide education and support for non-research staff in the delivery of protocol driven treatment for all patients. Participate in monitoring and audit activities within research team To carry out non-medical prescribing within scope of professional practice and in accordance with local policies and procedures and national legislation (optional and depending on clinical service needs). Personal Education, Training and Development Maintain professional development whilst evaluating own specialist knowledge and practice through a process of appraisal and personal development planning. Promote the role of the clinical research nurse as an integral part of the healthcare system. Increase and maintain awareness of current advances in cancer treatments, research and nursing practice thereby maintaining the highest standard of care for patients with cancer and implementing evidence-based care by continuing professional development. Participation in trust-wide education programs and study days. Obtain clinical supervision as appropriate. To keep up to date with departmental, Trust, UK and EU developments for the management of clinical research ensuring timely, effective implementation of changes. Attendance at team and divisional meetings. Staff Management and Development In conjunction with the team leader, provide the induction, continued supervision and management of the research teams. In conjunction with the team leader, be responsible for ensuring all members of the research nurse team undergo regular appraisal and support appropriate training and development opportunities in line with role requirements. Lead on the development of specialist study days within own research team Provide specialist education and training in relation to clinical trials to all key stakeholders. Disseminate information by attendance and /or presentations at local, national and international conferences/meetings Be responsible for the development of members of the research team.

The Christie NHS Foundation Trust is an international leader in cancer research and development and is one of the largest cancer treatment centre of its kind in Europe.

This post presents an exciting opportunity to join The Breast Research Team with an extensive portfolio of early to later phase trials.

Key responsibilities of the post include leadership and management of a group of research nurses supporting the Research Nurse Team Leader, ensuring research is conducted within requirements of a multiregulated clinical research environment safeguarding the wellbeing of patients, raising the profile of the clinical research nurse and clinical trials and ensuring Divisional, Trust and national objectives.



You will have excellent communication and interpersonal skills in line with The Christie values, possess strong motivation and have the ability to work independently. A background in oncology and research is essential, as it is experience in leadership and flexibility in working.You will interact with variety of research professionals across The Christie including the NIHR Manchester Clinical Research Facility as well as across Manchester and the wider networks.You should have a proactive approach to self-development as well as being able to demonstrate initiative and expertise in team development and wider training programmes.

An informal visit to discuss the post is highly recommended.

The Christie is one of Europe’s leading cancer centres, treating over 60,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 15% patients are referred to us from other parts of the country.

We provide radiotherapy through one of the largest radiotherapy departments in the world; chemotherapy on site and through 14 other hospitals; highly specialist surgery for complex and rare cancer; and a wide range of support and diagnostic services. We are also an international leader in research, with world first breakthroughs for over 100 years.

We run one of the largest early clinical trial units in Europe with over 300 trials every year. Cancer research in Manchester, most of which is undertaken on the Christie site, has been officially ranked the best in the UK.

DUTIES AND RESPONSIBILITIES

Clinical Research Co-ordination

· Work autonomously in all areas of practice relating to clinical research.

· Understand and deliver care in accordance with regulatory approved clinical research protocols.

· Oversee the process for obtaining NHS permissions (R&D approval) for clinical trials within team. As project lead, ensures permissions are in place prior to any patient recruitment.

· Undertake feasibility and risk assessments of clinical trial protocols in conjunction with Team Leader, Principal Investigator and Senior Clinical Trials Co-Ordinator

· Ensure all clinical trial activities are recorded in appropriate systems in a timely manner.

· Awareness of trial specific, regional, and national targets.

· Initiate new recruitment strategies for recruiting patients to clinical trials including engagement with the research network.

· In conjunction with Team Leader lead on the delegation of all trial related activities to research team members (clinical and administrative) and ensure compliance with SOPs and ICH/GCP.

· Work with team leader and sponsor companies in the preparation and negotiation of financial contracts for individual trials.

· Arrange and facilitate clinical trial related meetings.

· In conjunction with Team Leader, oversee appropriate financial remunerations for clinical trial activity



Clinical Service and Professional Responsibilities

· Assimilation of highly complex information relating to clinical trials and communication to patients at a level appropriate to their understanding. Ensure highly sensitive information is communicated to patients, relatives, and careers regarding prognosis

· Responsible for the development, implementation, and review of specialist care pathways in conjunction with appropriate personnel.

· Demonstration of expert knowledge in specialist area to maintain clinical excellence.

· Set up processes/patient pathways in conjunction with appropriate personnel from specialist research areas to promote a cost-effective timely service for individual protocols (shared care pathways, specialist clinics, etc.).

· Support Team Leader in delivering divisional and trust strategic objectives including performance indicators and metrics.

· Escalation of governance issues impacting on delivery of job purpose.

· To act as a primary contact point for the clinical trial patients and act as adviser to other health care professionals.

· Responsibility for maintenance and development of professional knowledge and practice by attending mandatory and specialist training (e.g., GCP) in accordance with local policy

· Ensuring care delivery standards in accordance with trial protocol, local policy, NMC Code of Practice Conduct and current best practice

· Development and maintenance of a high-quality service by:

o Overseeing the safe administration of all licensed and unlicensed medicinal products within the context of a clinical trial.

o Overseeing assessment and evaluation of treatment toxicities and initiation of appropriate intervention.

o Contribute to development of specialist Standard Operating Procedures and guidelines

· Provide education and support for non-research staff in the delivery of protocol driven treatment for all patients.

· Participate in monitoring and audit activities within research team

· To carry out non-medical prescribing within scope of professional practice and in accordance with local policies and procedures and national legislation (optional and depending on clinical service needs).



Personal Education, Training and Development

· Maintain professional development whilst evaluating own specialist knowledge and practice through a process of appraisal and personal development planning.

· Promote the role of the clinical research nurse as an integral part of the healthcare system.

· Increase and maintain awareness of current advances in cancer treatments, research and nursing practice thereby maintaining the highest standard of care for patients with cancer and implementing evidence-based care by continuing professional development.

· Participation in trust-wide education programs and study days.

· Obtain clinical supervision as appropriate.

· To keep up to date with departmental, Trust, UK and EU developments for the management of clinical research ensuring timely, effective implementation of changes.

· Attendance at team and divisional meetings.



Staff Management and Development

· In conjunction with the team leader, provide the induction, continued supervision and management of the research teams.

· In conjunction with the team leader, be responsible for ensuring all members of the research nurse team undergo regular appraisal and support appropriate training and development opportunities in line with role requirements.

· Lead on the development of specialist study days within own research team

· Provide specialist education and training in relation to clinical trials to all key stakeholders.

· Disseminate information by attendance and /or presentations at local, national and international conferences/meetings

· Be responsible for the development of members of the research team.


This advert closes on Monday 16 Sep 2024

Proud member of the Disability Confident employer scheme

We're looking for a full time Band 5 Clinical Research Practitioner to coordinate and deliver clinical research studies at The Christie NHS Foundation Trust.

We are looking for a highly motivated and enthusiastic individual who can contribute to the development of clinical research for people with cancer within the Rare Tumours Research Team. Our team work with Teenagers and Young Adults (TYA) and an interest in TYA would be an advantage. We look after patients with rare cancers including patients with CNS tumours and Sarcomas.

We have an extensive portfolio of trials, NIHR academic and commercial clinical trials, covering these disease groups. The role of the CRP will involve recruiting patients to these clinical trials, obtaining informed consent where appropriate, supporting patients enrolled in clinical trials, and ensuring study interventions are completed according to Good Clinical Practice (GCP) and Trust standards.

You will be working within a supportive team of experienced clinical research nurses and the clinical trial administration team.

The post will involve coordinating a portfolio of research studies across different specialties within the Trust and is ideal for individuals with an interest in TYA and experience of working in a busy clinical / research environment who wish to further develop their skills and experience.

We are seeking candidates with experience in working in clinical research in the NHS that can demonstrate knowledge of Good Clinical Practice and clinical skills, such as phlebotomy. Strong communication and organisational skills are essential, and a flexible working approach is a key element to this role.

The Christie is one of Europe’s leading cancer centres, treating over 60,000 patients a year. We are based in Manchester and serve a population of 3.2 million across Greater Manchester & Cheshire, but as a national specialist around 15% patients are referred to us from other parts of the country.

We provide radiotherapy through one of the largest radiotherapy departments in the world; chemotherapy on site and through 14 other hospitals; highly specialist surgery for complex and rare cancer; and a wide range of support and diagnostic services. We are also an international leader in research, with world first breakthroughs for over 100 years.

We run one of the largest early clinical trial units in Europe with over 300 trials every year. Cancer research in Manchester, most of which is undertaken on the Christie site, has been officially ranked the best in the UK.

DUTIES AND RESPONSIBILITIES:

The specific responsibilities will depend on the requirements of each team, but may include:

Clinical Research Delivery & Co-ordination

· To act as a primary contact point for the clinical trial patients for defined clinical trials and act as adviser to other health care professionals.

· Interview, recruit, take informed consent and support patients and carers in clinical trials/studies. This involves educating patients on the trials involved, explaining the advantages and disadvantages of taking part in trials, whilst always remaining unbiased.

· Ensure the provision of optimal patient care by alerting appropriate clinical colleagues when referral to other members of the MDT may be required.

· Be responsible for the safe and accurate collection of research samples and data, through clinical procedures such as venepuncture, and history taking, standard observations and other assessments including questionnaires, rated scales, qualitative interviewing as required by the protocol.

· Centrifuge, process, track and ship samples in line with protocol requirements

· Work with the clinical trials team and investigators to develop strategies to overcome barriers to recruitment and to solve other problems relating to specific studies

· Work with other departments within the Trust to ensure that trial specific investigations and procedures are undertaken as required by the trial protocol, to establish eligibility and safety of patients within clinical trials.

· Act as a key point of contact with the R&D core team, study sponsors, clinical research organisations and specific research teams.

· Manage the set up and initiation of allocated clinical trials within assigned Clinical Research Teams.

· Where delegated to do so, set up and maintain study site files in accordance with GCP and Trust SOPs.

· Understand and deliver protocols in accordance with regulatory requirements

· Ensure all clinical trial activities are recorded in appropriate systems in a timely manner.

· Maintain adequate patient records and ensure all relevant information is documented in the patient’s notes.

· Oversee and complete case report forms and participate in monitoring visits as per sponsor requirements.

· Ensure that all documents are archived in the appropriate way by following the Trust’s archiving guidelines.

· Undertake general administrative tasks as delegated by managerial representatives from the R&D division to contribute to the smooth running of the patient recruitment teams.

· Attend research team meetings to maintain an overview of team activity.

· Awareness of trial specific, regional and national targets. Identify and implement strategies for recruiting patients to clinical trials ensuring that targets for patient recruitment are delivered.



Clinical Service Responsibilities

· Demonstrate awareness of divisional and trust strategic objectives including performance indicators and metrics.

· Escalation of governance issues impacting on delivery of job purpose.

· Participate in monitoring and audit activities within research team

Management

· Provide induction support and training to new and existing clinical trials staff, including development of training sessions and guidance documents.

· Encourage the sharing of best practice and dissemination of information through regular structured meetings with all trials administration staff.

· Assist with metric tracking for performance indicators including mandatory training requirements, divisional key performance indicators (i.e. time to recruiting first patient from NHS permission, patient recruitment to time and target), amendment timelines and divisional absences.



PERSONAL AND PEOPLE DEVELOPMENT

· Maintain professional development whilst evaluating own specialist knowledge with assistance from their assigned line manager to satisfy the NHS Knowledge and Skills Framework.

· Participate in and deliver Trust-wide education programmes and study days, regional and national meetings and research seminars as appropriate.



PHYSICAL, MENTAL AND EMOTIONAL EFFORT

· Long periods of time spent using keyboard to input information and use of VDU for electronic communication.

· Prolonged concentration is regularly required (e.g. when checking through trial documentation and entering data into spreadsheets).

· Occasional exposure to distressed circumstances as trial patients are commonly suffering from terminal illnesses.


This advert closes on Thursday 26 Sep 2024

Proud member of the Disability Confident employer scheme

A 1- year fellowship has been created to allow the successful candidate to gain specialist training in advanced radiotherapy. The particular emphasis of this fellowship will be towards the technological advances in Radiation Oncology. The fellowship will allow the candidate to gain in depth experience in advanced radiotherapy techniques such as IMRT (intensity-modulated radiotherapy) and advanced image-guided radiotherapy using the MR-Linac. There will also be the opportunity to gain research experience and pursue original research projects.
This is an opportunity for the candidate to launch a career in world-leading cancer research. They will play a part in improving treatment-decision making for patients with locally advanced Non-Small Cell Lung cancer (NSCLC) by identifying biomarkers that can be used to stratify patients in future clinical trials. A range of high- quality data has already been collected in the VIGILANCE study including ctDNA patterns, radiomics features from imaging and electronic patient reported outcome measures (ePROMs). Their role will be part of our overall strategy to make more use of routinely collected data to personalise treatment approaches and improve patient outcomes for all.
We are looking for candidates with ambition, commitment, a passion to improve patient outcomes and a strong desire to develop a career in cancer research.

This position is suitable for individuals who wish to gain specialist training in advanced radiotherapy research. The post holder is required to have obtained a FRCR qualification or equivalent prior to commencing this post.
This post is for 40 hours per week to provide support for the appropriate clinics and research that is taking place in the department of Radiotherapy Related Research Group.
The post holder will also play an active role in the recruitment of patients onto lung cancer clinical trials and in all aspects of care for patients enrolled on these trials. They will work closely with other members of the multidisciplinary teams and will support the consultants, clinical fellows, specialist registrars, and clinical research nurses in managing the clinical trial portfolio of the Lung Cancer Research Team.

It is anticipated the post-holder will attend appropriate clinics per week (a maximum of one research and one NHS clinics), and multidisciplinary meetings. In addition, they will participate in clinical research meetings and any other relevant trial planning or trial set-up meetings. The post-holder will also spend time analysing clinical data, writing abstracts/manuscripts, planning new studies and attending educational meetings.

The Lung team comprises 9 Consultants, 2 Sub-specialty Trainee and 2 Clinical Fellows. We are supported by a team of 4 Clinical Nurse Specialists. We are friendly, hard-working team focused on delivering high quality patient-centred care. We encourage all members of team to engage in SMDT, clinics and inpatient care.
We have a team of 8 research radiographers led by a team leader who implement radiotherapy (RT) clinical trials including access to advanced technologies such as MR-Linac and protons.
On average, the team can be managing 20 recruiting studies and 20 studies in follow-up with Principal Investigators across clinical oncology and surgery.
We have access to a National Institute for Health Research Clinical Research Facility on-site. This facility gives us access to a dedicated unit to treat patients on trials and a research laboratory to process clinical
The Radiotherapy Related Research department has world-leading collaborative researchers in RT immunology, radiobiology, biomarkers, pre-clinical drug RT combination studies, RT physics, computational oncology and Proton Beam Therapy. Its ambition is to drive Phase I-III clinical trials with state-of-the art radiotherapy, alongside imaging and biological prognostic and predictive biomarker development including genomics, transcriptomics and proteomics.

Duties

1. Recruit patients for the VIGILANCE study, analyse the data and present the findings. This role also involved conducting translational research in collaboration with CRUK National Biomarker Centre.
2. Work with other clinical oncologists, physicians, radiotherapy planning specialists, physicists, methodologists, and statisticians to ensure a collaborative working
3. Be involved in the clinical management of lung cancer patients receiving radiotherapy environment.
4. Interact with allied research activities.
5. Supervise entry and treatment of patients in clinical studies
6. Support the Lung Cancer Research Team in the delivery of clinical trials.
7. Undertake projects related to radiotherapy-related research including patient recruitment, data analysis, protocol and grant writing.
8. Produce, or contribute towards, high impact peer-reviewed publications.
9. Disseminate research findings through presentations at seminars and conferences.

Line Management

The post holder will be responsible to Professor Corinne Faivre-Finn, Professor of Thoracic Radiation Oncology, University of Manchester/Honorary Consultant in Clinical Oncology, The Christie NHS Foundation Hospital




This advert closes on Wednesday 11 Sep 2024

Proud member of the Disability Confident employer scheme

Equipment performance testing and radiation protection surveys (main focus of role) Undertakes equipment performance and radiation protection surveys, alone or with a colleague, following standard operating procedures defined within an ISO9001 quality system: Performs routine quality control on existing installations Assists in the critical examination and commissioning of new equipment to ensure that it is safe for bringing into clinical use Assists with investigation of faults on existing installations Calibrates patient dose measuring equipment to confirm the accuracy of recorded dose Checking the radiation protection of the installation to ensure staff and public safety This will involve accurate positioning and methodical use of test objects. Analysing the results of equipment performance measurements Write electronic reports for the Radiation Protection Advisor/Medical Physics Expert and customers, detailing findings and recommending actions required Calibrating x-ray dose measuring equipment Perform testing of UV units, as required by the group. Providing advice on level A QC testing, review results and report findings. Radiation Protection Assist in providing radiation protection advice and support as required in the team. This includes producing ad hoc reports on equipment or customer sites, e.g. lists of equipment due, inter-comparison of similar equipment types Updating central records of measurements, e.g. typical patient doses, equipment calibration factors Calibrating radiation protection meters as required and/or organising dispatch of equipment for external calibration. Supervision and responsibilities for information resources Maintains accurate records using Excel and Access (or other databases as rolled out in the NHS), e.g. results from testing, details of equipment Liaise with radiographic staff to book survey visits in conjunction with the Booking Team as required Supervise less experienced healthcare science staff (assistants, associates, practitioners or scientists) when undertaking equipment performance and radiation protection surveys as part of their training. Undertake internal audits. A take a lead on a number of group functions such as H&S checks, oversight of online QA platforms, maintaining our inventory etc, as required Professional Undertakes training identified as required for role, including continuing professional development Gains and maintains registration as clinical technologist Follow the appropriate key work instructions, risk assessments and systems of work and ensure direct supervision of those you are responsible for until they are competent. Collaborates with other members of the group in the improvement of test protocols. Contributes to the teaching (and outreach) commitments of the service such as assisting in the preparation and delivery of material, e.g. at the Radiation Protection Supervisors courses. Contributes to the research and development of the service, e.g. by carrying out measurements or processing data

DUTIES AND RESPONSIBILITIES: Clinical Research Co-ordination Work under supervision in all areas of practice relating to clinical research. Understand and deliver care in accordance with regulatory approved clinical research protocols. Understand the process for obtaining NHS permissions (R&D approval) and for conducting clinical trials at site. Has an awareness of the requirement to ensure that all clinical trial activities are recorded in appropriate systems in a timely manner. Support the research team with the conduct of studies within set competencies and in accordance with regulatory approved clinical research protocols. Attend clinical trial related meetings where appropriate. Clinical Service and Professional Responsibilities With the oversight of a senior clinical research nurse understand protocol design and be able to deliver care in accordance with a clinical trial protocol. Support patients and their carers when receiving complex and sensitive information in relation to their treatment and prognosis. Demonstration of research knowledge when caring for patients receiving treatment within the context of a clinical trial protocol. Report incidents using hospital systems and be aware of appropriate health and safety policies to refer as required. To act as a contact point for the clinical trial patients and other members of the multi-disciplinary team. Responsible for maintenance and development of professional knowledge and practice by attending mandatory and specialist training in accordance with local policy. Deliver care in accordance with trial protocol, local policy, NMC Code of Practice Conduct, GCP and current best practice. Maintenance of a high-quality service by: The safe administration of all licensed and unlicensed medicinal products within the context of a clinical trial. The assessment and evaluation of treatment toxicities + escalation of concerns as appropriate Assist in the provision of education and support for non-research staff in the delivery of protocol driven treatment for all patients. Participate in monitoring and audit activities within research team as required Have an awareness of the risk assessment process in relation to clinical trials. Personal Education, Training and Development Maintain professional development whilst evaluating own specialist knowledge and practice through a process of appraisal, reflective practice and personal development planning. Support senior colleagues in raising awareness of the role of the clinical research nurse as an integral part of the healthcare system. Maintain awareness of current advances in cancer treatments, research and nursing practice thereby maintaining the highest standard of care for patients with cancer and implementing evidence-based care by continuing professional development. Participation in trust-wide education programmes and study days. Obtain clinical supervision as appropriate. To keep up to date with departmental, Trust, UK and EU developments for the management of clinical research ensuring timely, effective implementation of changes. Attendance at team and clinical research nurse meetings. Staff Management and Development Support the development of specialist study days within own research team. Assist in the provision of specialist education and training in relation to clinical trials to all key stakeholders including student nurses. Disseminate information by attendance and /or presentations at meetings where appropriate. Contribute to the development of members of the research team Participate in appraisals (own and others) and work to achieve personal objectives

Clinical Research Fellow in hepatopancreaticobiliary and neuroendocrine neoplasms

This role will allow senior medical trainees to work within the hepatopancreaticobiliary and neuroendocrine neoplasm disease group at The Christie NHS Foundation Trust. This coordinated research expansion plan sits under the umbrella of the Systemic Therapy Research Group, which aims to substantially increase research output within the Department of Medical Oncology, through increased delivery of innovative investigator-led studies driven by The Christie NHS Foundation Trust. A key part of this process is to encourage education and empowerment of research staff at all levels, which includes training the next generation of cancer research leaders.
• These positions are suitable for enthusiastic and research-motivated applicants with a Medical degree, who are pursuing a career in Medical Oncology and have an interest in gaining further research and clinical trial experience in Hepatopancreaticobiliary and neuroendocrine neoplasms.

Candidates must hold full General Medical Council (GMC) registration and have International English Language Testing System (IELTS) proficiency at the time of post commencement, as appropriate. This Fellowship is a two year, full-time position, to support clinical research in this disease group and to provide specialist experience and training in the relevant disease areas for the successful applicants.

Depending on the projects, the successful applicant will need to divide their time between research and a moderate clinical commitment; this may involve clinical research and audit activities, including protocol-writing.

The post will be based within the Department of Medical Oncology under the supervision of a consultant clinician.

The post-holder will work closely with other members of the respective multidisciplinary teams and will support the consultants, clinical fellows, specialist registrar, nurses, nurse clinicians, trial co-ordinators and clinical research nurses in managing the disease group clinical trial portfolios. This will facilitate more rapid clinical decision making, an increase in the number of trials opened, together with increased recruitment of patients into new and existing research protocols.

Fellows will attend appropriate clinics per week (a maximum of two research and two NHS clinics), and multidisciplinary meetings. In addition, they will participate in clinical research meetings and any other relevant trial planning or trial set-up meetings. Fellows will also spend time reviewing clinical data, writing abstracts/manuscripts, planning new studies and attending educational meetings.

The disease sites treated by the hepatopancreaticobiliary and neuroendocrine disease group include hepatocellular carcinoma, pancreas cancer, biliary tract cancers [cholangiocarcinoma and gallbladder cancer] and neuroendocrine neoplasms (NENs). The group has an active clinical research programme (Phase I-III), with close links with basic research laboratories in the Cancer Research UK Manchester Institute. There are around 500 new patient HPB/NEN referrals received per year and approximately 25% of all patients are entered into clinical trials.

This group has an international reputation in the treatment of patients with NENs and is accredited as a Centre of Excellence by the European NET Society (ENETS). The fellow will have the opportunity to gain clinical experience in the management of patients with a HPB and NEN diagnosis in this world-leading specialist centre. In addition, the candidate will be encouraged and supported to become actively involved in the research activities of the unit and to undertake audits, service evaluation or quality improvement projects, develop proposals for grant applications and become involved in on-going clinical and translational research, and will be encouraged to develop their own projects and clinical trials, with the goal of presenting this work in abstract (national and international) and manuscript form.

DUTIES AND RESPONSIBILITIES

Depending on the projects, the successful applicant will need to divide their time between research and a moderate clinical commitment; this may involve clinical research and audit activities, including protocol-writing.

The post will be based within the Department of Medical Oncology under the supervision of a consultant clinician.

The post-holder will work closely with other members of the respective multidisciplinary teams and will support the consultants, clinical fellows, specialist registrar, and clinical research nurses in managing the disease group clinical trial portfolios. This will facilitate more rapid clinical decision making, an increase in the number of trials opened, together with increased recruitment of patients into new and existing research protocols.

Fellows will attend appropriate clinics per week (a maximum of two research and two NHS clinics), and multidisciplinary meetings. In addition, they will participate in clinical research meetings and any other relevant trial planning or trial set-up meetings. Fellows will also spend time reviewing clinical data, writing abstracts/manuscripts, planning new studies and attending educational meetings.

Key accountabilities

Clinical Research fellows will have the following opportunities within the Department of Medical Oncology:
• Audit:Fellows play a key role in Clinical Audit as a member of The Christie Medical staff.
• Clinics: Research fellows in Medical Oncology usually attend a number of outpatient clinics per week (seeing new referrals, follow-ups and patients on clinical trials) and are expected to undertake the administrative duties associated with the care of these patients.
• Clinical Governance:Fellows are expected to participate in all relevant aspects of clinical governance, including maintaining up-to-date protocols, guidelines and clinical audit, under the supervision of the Consultants in the disease group.
• Education:There are numerous courses organised annually by the School of Oncology at The Christie. Please refer to The School of Oncology website:http://www.christie.nhs.uk/school-of-oncology.aspx

In addition, there is an annual research event where all Medical Oncology fellows are encouraged to present their on-going research and a little about themselves. There are also weekly teaching sessions in practical life skills related to Medical Oncology, such as interview skills, oral presentation skills, curriculum vitae preparation, media training, career development etc.
• Professional Development: Fellows should also maintain a level of continuing professional development consistent with the recommendations of the Royal College of Physicians. Appropriate arrangements for study leave will be made in conjunction with colleagues. There is the potential to attend national/international meetings (when this is an option) to present research work and fellows are expected to be involved in writing papers and reviews, and will also be required to undergo an annual appraisal.
• Protocol Development:Fellows may also assist with the revision and development of evidence-based clinical trial protocols for patients.
• Research:There are excellent opportunities for research within the Department. Fellows are encouraged to contribute to current research projects within the unit and/or set up new projects. The Manchester Cancer Research Centre has been established to bring together the expertise, ambition and resources of partner organisations, which include the University of Manchester, the Cancer Research UK Manchester Institute, Cancer Research UK, in addition to The Christie NHS Foundation Trust.

Post holders are committed to delivering at least four of the following:
• Successfully complete a clinical audit.
• Actively participate in at least one national or international meeting (abstract presentation).
• Successfully publish at least two first-author peer-reviewed manuscripts.
• Aid income generation through assistance in development and writing of investigator-led studies/grant applications for research projects.
• Increase the international profile of the Disease Group, The Christie School of Oncology and The Christie Medical Oncology Fellowship programme.
• Representation from The Christie on international professional committees


This advert closes on Thursday 5 Sep 2024

Proud member of the Disability Confident employer scheme

We are seeking a motivated, methodical Healthcare Science Practitioner (Clinical Technologist) with problem solving skills to join our x-ray equipment evaluation team. The successful applicant will join a growing team of ~30 - scientists, technologists and administrators - providing equipment quality assurance and scientific support to NHS and independent sector radiology departments in the North West of England (a few customers are further afield).

The successful candidate will be assisting in all aspects of the service, including regular travel to customer sites (occasional overnight stays) to provide performance testing on a variety of diagnostic imaging equipment (e.g. dental, CR&DR radiographic and fluoroscopic), radiation protection surveys of diagnostic radiology installations and calibration of radiation instruments. When not working off-site they will be analysing data and producing reports, assisting with training of staff and customers.

Candidates should have scientific and interpersonal skills. There is a need for good communication skills to be able to work with colleagues in physics and radiology and professional behaviours are expected. Proactive team working is essential as well as the ability to work independently.

A current valid driving licence and a willingness to travel is essential to the role.

Undertakes level B (physics) equipment performance and radiation protection surveys. Writes reports detaining findings and making recommendations. Investigates concerns where they arise. Takes ownership of the quality of their work.

A working understanding of x-ray equipment, radiation instrumentation (such as dosemeters) and the relevant UK ionising radiation regulations and guidance/standards will be expected

Calibrates x-ray dose measuring equipment

Providing advice on level A (radiographer) QC testing, review results and report findings. Training andsupporting customers to fulfil their QC requirements for equipment.

Support senior practitioners and scientists in aspects of regulatory compliance at The Christie and in the North West region. Taking a lead in a small aspect of organisation for the team as required.

Applicants should be registered with the RCT as a Clinical Technologist or the HCPC as a Healthcare Science Practitioner (or eligible for these registrations) and have experience in the use of a range of X-ray imaging equipment.

Suitable applicants without knowledge/skills/experience (or registration) will be considered for appointment at band 4 while training (see job description).

We are the Diagnostic Radiology and Radiation Protection Section of the Imaging Physics and Radiation Protection Group within CMPE, based at The Christie in Manchester.

We have a large, fast paced service with opportunities for service development in response to government strategies around imaging capacity, workforce growth, role advancement, uptake of digital tools and efficient/flexible teams. Due to the size of the regional service we have access to an extensive portfolio of equipment with a focus on diagnostic/interventional radiology. Continued professional development is essential and supported.

Manchester is a hub for sport, music and culture as well as a friendly, vibrant city. The Christie is located 4 miles to the south of the City, in close proximity to Didsbury and Chorlton where there are many independent shops, restaurants and bars. There are a number of National Parks nearby and, for travelling further afield, Manchester International Airport (with flights to over 200 destinations) is minutes away while London is only 2 hours by train.

Additional information about the group can be found via The Christie website at Christie Medical Physics and Engineering

Equipment performance testing and radiation protection surveys (main focus of role)
• Undertakes equipment performance and radiation protection surveys, alone or with a colleague, following standard operating procedures defined within an ISO9001 quality system:
• Performs routine quality control on existing installations
• Assists in the critical examination and commissioning of new equipment to ensure that it is safe for bringing into clinical use
• Assists with investigation of faults on existing installations
• Calibrates patient dose measuring equipment to confirm the accuracy of recorded dose
• Checking the radiation protection of the installation to ensure staff and public safety
• This will involve accurate positioning and methodical use of test objects.
• Analysing the results of equipment performance measurements
• Write electronic reports for the Radiation Protection Advisor/Medical Physics Expert and customers, detailing findings and recommending actions required
• Calibrating x-ray dose measuring equipment
• Perform testing of UV units, as required by the group.
• Providing advice on level A QC testing, review results and report findings.

Radiation Protection
• Assist in providing radiation protection advice and support as required in the team.
• This includes producing ad hoc reports on equipment or customer sites, e.g. lists of equipment due, inter-comparison of similar equipment types
• Updating central records of measurements, e.g. typical patient doses, equipment calibration factors
• Calibrating radiation protection meters as required and/or organising dispatch of equipment for external calibration.

Supervision and responsibilities for information resources
• Maintains accurate records using Excel and Access (or other databases as rolled out in the NHS), e.g. results from testing, details of equipment
• Liaise with radiographic staff to book survey visits in conjunction with the Booking Team as required
• Supervise less experienced healthcare science staff (assistants, associates, practitioners or scientists) when undertaking equipment performance and radiation protection surveys as part of their training.
• Undertake internal audits.
• A take a lead on a number of group functions such as H&S checks, oversight of online QA platforms, maintaining our inventory etc, as required

Professional
• Undertakes training identified as required for role, including continuing professional development
• Gains and maintains registration as clinical technologist
• Follow the appropriate key work instructions, risk assessments and systems of work and ensure direct supervision of those you are responsible for until they are competent.
• Collaborates with other members of the group in the improvement of test protocols.
• Contributes to the teaching (and outreach) commitments of the service such as assisting in the preparation and delivery of material, e.g. at the Radiation Protection Supervisors courses.
• Contributes to the research and development of the service, e.g. by carrying out measurements or processing data


This advert closes on Wednesday 4 Sep 2024

Proud member of the Disability Confident employer scheme