Total 253 Science / R&D / Research job vacancies in bury greater manchester bl9 0ex

• Start date: ASAP
• Full-time and long-term position
• Teaching all 3 Sciences at KS3 & KS4
  
  We are working in partnership with an Ofsted 'Good' 11-16 secondary school in Manchester who are seeking an enthusiastic and committed Science Teacher to join their team for the new academic year. This is a full-time and long-term job. There is a temporary to permanent opportunity for the right candidate. Due to this being a long-term job, full teaching responsibilities will be required, including planning and marking.
  
  Job Description
• Delivering engaging and creative Science lessons to students in Key Stages 3 and 4.
• Planning and preparing schemes of work, lesson plans, and assessments.
• Monitoring student progress and providing feedback.
• Contributing to the development of the department's curriculum.
• Participating in extracurricular activities such as science/STEM clubs and school trips.
  
  Requirements
• Qualified Teacher Status (QTS) or equivalent. ECT's welcome to apply.
• Bachelor's degree in science or related field
• Recent experience teaching Science at secondary school level.
• Strong behaviour/classroom management.
• Ability to work collaboratively with other teachers and staff members
  
  If you are interested in this role, contact Abbie Albison at Hays Education by applying via this website or email
  **Hays Education are currently recruiting Qualified Secondary Teachers for several long term/permanent teaching roles around Greater Manchester. Refer a Friend/Colleague and Hays can issue £350 vouchers for every successful appointment.
  
  We look forward to hearing from you!

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

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

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.

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

Fantastic opportunity for graduates! Are you passionate about creative writing, research and technology? We are looking for Graduate Research Analyst to join a growing tech consultancy company in London. This role offers an excellent opportunity for recent graduates to develop their analytical skills and contribute to meaningful projects.

Graduate Research Analyst (based in London, Salary: £22k - £30k DOE)

Here's what you'll be doing:

- Conducting research on various topics, industries, and markets to gather relevant data and insights.
- Analysing data using statistical techniques and software tools to extract valuable information.
- Assisting in the preparation of reports, presentations, and summaries based on research findings.
- Collaborating with team members to identify key research objectives and deliverable
- Leveraging AI to develop solutions that align with commercial goals, making impacts

Who you are:

- An academic passionate about learning and eager to explore new frontiers of knowledge.
- A talented writer who excels at turning thoughts into captivating tales.
- A tech lover always on the lookout for fresh solutions to longstanding problems
- A curiosity for AI

Here are the skills you'll need:

- Strong analytical skills with the ability to interpret complex data sets
- Effective communication skills, both written and verbal
- Proficiency in statistical analysis tools
- Attention to detail and accuracy in data analysis and reporting

Here are the benefits of this job:

- Competitive salary between £22k - £30k depending on experience
- Opportunities for professional development and career growth.
- Collaborative work environment that fosters innovation and creativity.
- The chance to grow within multidisciplinary environment
- Competitive rewards with an opportunity to be at the forefront of technology and research

Work Permissions: You must have the right to work in the United Kingdom. Visa sponsorship is not available at this time.

Your new company
Due to a high demand for Science Teachers across Salford andsurrounding areas, Hays Education are looking to register a number of Scienceteachers of all experience levels.
Your new role
You will be responsible for teaching your Science discipline, orin some cases across all 3 areas at Secondary schools across GreaterManchester.
In a long term role you will be responsible for planning anddelivering lessons, as well as completing the subsequent marking and assessmentof pupils work, ensuring all pupils are progressing well within the classroom.You will also be expected to attend and prepare for Parents Evenings throughoutthe academic calendar.

Behaviour management will also be your priority, as well asensuring pupils are achieving to the best of their ability and engaging withthe subject in your classroom.
What you'll need to succeed
In order to be a registered teacher with Hays Education, you mustpossess QTS / QTLS and ideally have experience of teaching your 1 Sciencediscipline, or teaching all 3 Sciences across KS3 and KS4.

You must give full commitment to the role that you accept, andshow your work ethic and flexibility to adjust to your new environment.
What you'll get in return
You will have a dedicated and supportive Hays Consultant who willbe in contact with you throughout the duration of the contract, and in additionto this, you will also be invited to join our Hays Education Hub App which ishow we will send out newly registered jobs tailored to you. This will also giveyou access to unlimited free training courses, as well as being able to updateyour availability at any time via the app.
You will also join our Hays Refer a Friend Scheme where you couldbe entitled to receiving £350 in high street vouchers.
You will be able to use the Hays Timesheet App or online system tosubmit your timesheets each week.

There is also a potential that long term positions are extended aswell as made permanent, depending on the situation of the role / school.
What you need to do now
If you are interestedin this role, contact Abbie Albison at Hays Education by applying via thiswebsite or email

**Hays Education arecurrently recruiting Qualified Secondary Teachers for several longterm/permanent teaching roles around Greater Manchester. Refer aFriend/Colleague and Hays can issue £350 vouchers for every successfulappointment.

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

Your new company
Due to a high demand for Science Teachers across Bolton andsurrounding areas, Hays Education are looking to register a number of Scienceteachers of all experience levels.
Your new role
You will be responsible for teaching your Science discipline, orin some cases across all 3 areas at Secondary schools across GreaterManchester.
In a long term role you will be responsible for planning anddelivering lessons, as well as completing the subsequent marking and assessmentof pupils work, ensuring all pupils are progressing well within the classroom.You will also be expected to attend and prepare for Parents Evenings throughoutthe academic calendar.

Behaviour management will also be your priority, as well asensuring pupils are achieving to the best of their ability and engaging withthe subject in your classroom.
What you'll need to succeed
In order to be a registered teacher with Hays Education, you mustpossess QTS / QTLS and ideally have experience of teaching your 1 Sciencediscipline, or teaching all 3 Sciences across KS3 and KS4.

You must give full commitment to the role that you accept, andshow your work ethic and flexibility to adjust to your new environment.
What you'll get in return
You will have a dedicated and supportive Hays Consultant who willbe in contact with you throughout the duration of the contract, and in additionto this, you will also be invited to join our Hays Education Hub App which ishow we will send out newly registered jobs tailored to you. This will also giveyou access to unlimited free training courses, as well as being able to updateyour availability at any time via the app.
You will also join our Hays Refer a Friend Scheme where you couldbe entitled to receiving £350 in high street vouchers.
You will be able to use the Hays Timesheet App or online system tosubmit your timesheets each week.

There is also a potential that long term positions are extended aswell as made permanent, depending on the situation of the role / school.
What you need to do now
If you are interestedin this role, contact Abbie Albison at Hays Education by applying via thiswebsite or email

**Hays Education arecurrently recruiting Qualified Secondary Teachers for several longterm/permanent teaching roles around Greater Manchester. Refer aFriend/Colleague and Hays can issue £350 vouchers for every successfulappointment.

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

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 looking for highly motivated nurse to join the Experimental Cancer Medicine Team (ECMT) at The Christie NHS Foundation Trust. ECMT supports a growing portfolio of early phase research studies both commercial and investigator led, including first in human drug trials.

The post holder will work alongside a team of physicians, research nurses & clinical trial administrators on a portfolio of trials providing support to patients, administering trial treatments & carrying out trial assessments for patients on study.

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.

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 coordination of the trial protocols and support for cancer patients.

A background in oncology, flexibility in working, excellent communication and interpersonal skills are essential. Experience in clinical research would be desirable but not essential.
An informal discussion about the post is strongly recommended with the possibility to spend some time with the team to understand better the requirements of the role.

The CRN will be involved in varied portfolio activities including clinical care of patients, patient recruitment and management, supporting team with data query resolution, reviewing protocol amendments, providing patient-centred insights to the research delivery team by supporting both the patients and the team through all aspects of clinical research in the ECMT research team.

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.

By utilising national frameworks for auditing patients experience the CRN will ensure patients will have the best possible experience whilst participating in clinical research.

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.

Demonstrate awareness and contribution to divisional, Trust and national objectives and strategies.

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 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:

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

Ø 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


This advert closes on Wednesday 4 Sep 2024

Proud member of the Disability Confident employer scheme

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

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

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

DUTIES AND RESPONSIBILITIES Planning and Organisation Contribute to the strategic planning of observational and supportive care team projects and developments, identifying interdependencies across projects/functions, potential impacts on wider organisation, resource requirements and building in contingency and advising on necessary adjustments. Contribute to the development of performance and governance strategies and support the development and implementation of improvement programmes, in accordance with local and Divisional priorities Contribute to development and achievement of short-, medium- and long-term business plans and objectives Organise and schedule research meetings, ensuring appropriate accommodation, attendance and distribution of papers, and that an agenda is agreed Coordinate, manage and monitor work flow within the observational and supportive care team in collaboration with RM/clinical leads Policy and Service Development Contribute to the review of existing services to promote development of the observational and supportive care team services Where appropriate develop operational procedures in collaboration with the quality assurance leads Support the directorate operational leads in service development plans to align with national and local strategic priorities Performance Management Contribute to the development and maintenance of the infrastructure to measure and monitor performance within the observational and supportive care team to ensure that performance is in line with key performance indicators Optimise working practices to maintain and continuously improve efficiencies within the observational and supportive care team in collaboration with key stakeholders Participate in the monitoring of compliance with all relevant standards Business Planning and Financial Management Support the development and production of business plans for services/projects as required Analyse and interpret complex data in order to deliver well-presented information Support clinical leads and business planning to ensure targets are met to maximise income. Support the use of service line reporting to inform financial management Liaise with relevant stakeholders in the development of grant applications Management and Leadership Direct line management responsibility for non-clinical staff within the observational and supportive care team including administrative workload allocation Provide leadership within the observational and supportive care team and act as a role model and resource for all team members Responsible for recruitment, retention, disciplinary and grievance, and all staffing management issues in accordance with relevant Trust policies Contribute to the delivery of training programmes Work collaboratively to identify and meet the learning needs of observational and supportive care team members Maintain own and professional development and identify learning needs and opportunities Information Management Working collaboratively to ensure that all relevant internal and external stakeholders are provided with high-quality, timely, well-presented and relevant data reports supporting stakeholders in understanding operational efficiency, performance against national and local targets, activity and financial performance, and service size, configuration and potential for growth. Establish working practices to ensure data is accurately collated and maintained, including externally facing information e.g., web pages Ensure research outputs are communicated appropriately Communication Communicate complex research information in written and oral format to internal and external parties Work, liaise and communicate with colleagues across the Trust, including service support areas to improve the delivery and quality of research and research services Where appropriate attend observational and supportive care team meetings to present information. Represent the observational and supportive care team projects at national conferences and workshops, leading on presentations as required. Work collaboratively within all teams in the Division of Research to maintain and enhance partnerships withpharmaceutical companies, other NHS sites and academia.

• Start date: September 2024
• Full-time and long-term position
• Teaching all 3 Sciences at KS3 & KS4
  
  We are working in partnership with a secondary school in Manchester who are seeking an enthusiastic and committed Science Teacher to join their team for the new academic year. This is a full-time and long-term job. There is a temporary to permanent opportunity for the right candidate. Due to this being a long-term job, full teaching responsibilities will be required, including planning and marking.
  
  Job Description
  Delivering engaging and creative Science lessons to students in Key Stages 3 and 4.
  Planning and preparing schemes of work, lesson plans, and assessments.
  Monitoring student progress and providing feedback.
  Contributing to the development of the department's curriculum.
  Participating in extracurricular activities such as science/STEM clubs and school trips.
  
  Requirements
  Qualified Teacher Status (QTS) or equivalent. ECT's welcome to apply.
  Bachelor's degree in science or related field
  Recent experience teaching Science at secondary school level.
  Strong behaviour/classroom management.
  Ability to work collaboratively with other teachers and staff members
  
  If you are interested in this role, contact Abbie Albison at Hays Education by applying via this website or email
  **Hays Education are currently recruiting Qualified Secondary Teachers for several long term/permanent teaching roles around Greater Manchester. Refer a Friend/Colleague and Hays can issue £350 vouchers for every successful appointment.
  We look forward to hearing from you!

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