Total 16 job vacancies by NHS Jobs

To deliver on-going developmental, education and training programs for all pharmacy staff. Designing and implementing appropriate teaching, learning and assessment plans to support trainee pharmacists, in line with local, regional and national agendas. Provide educational or practice supervision for all trainees as required. Support others to deliver on training curriculums in their roles as educational or practice supervisors. Develop or maintain partnerships with higher education institutes. Develop or maintain partnership with regional and local organisations to advance the education and training strategy. To support in education and training of non-pharmacy staff within the organisation To deputise for the Lead Pharmacist for Education and Training where required Work as a clinical pharmacist if appropriate providing a service to a defined cohort of patients To undertake a clinical area of responsibility as part of enabling non-medical prescribing training and to maintain own clinical competence. Where required, act as a designated prescribing practitioner for trainee pharmacists from September 2025 onwards. To support in the promotion of pharmacy and pharmacy careers to external organisations Line manages designated pharmacists, trainee pharmacists or other members of the pharmacy team. Undertake audits and engage with Quality Improvement and practice research projects As a Practice Educator, work within realms of specialist therapeutic knowledge and experience and teach therapeutic topics as well general areas of pharmacy practice, as applicable The post holder will contribute to teaching on the new University of Bath MPharm delivered at the University of Plymouth: Practice Educators will work in two different workplaces: clinical pharmacy practice (hospital) and the University of Plymouth campus. To make this arrangement work there is recognition from both workplaces of the for flexibility. The university workload is driven by term dates and the preferred arrangement is for Practice Educators to work the equivalent of 0.5 WTE on the following basis:- 3 days a week during term time- 2 days a week outside of term time Most of the teaching is timetabled for 9am 5pm but may be timetabled up until 7pm. Therefore, Practice Educators will need to be available between 9am and 5pm with occasional flexible working to cover timetabled late sessions. Annual leave should be taken outside of term time where possible.

Assess, plan, implement and evaluate treatment safely and effectively, in partnership with medical team and nurses, service user and carers, using evidence-based practice. To ensure comprehensive risk assessment of patients and risk management plans are in place and clearly documented in accordance with the Trusts Policy. Manage and assess risk within the areas of responsibility, ensuring adequate measures are in place to protect self, colleagues, and patients. Monitor work areas and practices to ensure they are safe and free from hazards and conform to health, safety and security legislation, policies, procedures, and guidelines. Act as a specialist advisor/professional leader in healthcare issues related to the care of the patient with learning disability which can often be complex and urgent. Prioritise health problems and intervene appropriately to assist the patient in complex, urgent or emergency situations, including initiation of effective emergency care. As part of the team provide regular updates, feedback, and reports to senior management on progress and share any identified barriers that may need to be addressed in order to meet plans and targets Undertake risk assessments and escalate in line with Trust Policies and guidelines. Report any observed changes in a patients condition or behaviour, or any other cause for concern, to an appropriate clinician as a key health and wellbeing responsibility. Refer to colleagues or other agencies as appropriate, this will include any identified concerns around risks, health inequalities and safeguarding. 5.1 Responsibility for People Management Provide line management and caseload supervision to other members of team where appropriate Maintain professional registration. To participate in regular supervision and performance management development and appraisal processes To participate in regular clinical supervision sessions in order to received professional support and time to reflect upon practice Act as a mentor to students and colleagues, participating in induction programmes, guiding practice, and assessing competence to develop staff. Provide teaching sessions within the team and across the Devon ISC as appropriate on relevant topic relating to screening and learning disabilities. Deliver specialist training for Primary health care and community staff in new skills related to health screening uptake in patients with a learning disability. To participate in regular clinical supervision sessions to receive professional support and time to reflect upon practice. Take responsibility for own development, learning and performance including participating in clinical supervision and training as necessary to update skills and knowledge and maintaining a record of own personal development. Provide advice and highly specialist support to all healthcare professionals who are providing care to individuals with a learning disability, ensuring reasonable adjustments are made to facilitate access to both primary, secondary and community care. Working with local learning disability groups to understand language barriers and undertake collaborative works to identify and overcome any identified barriers that may be contributing to health inequalities and uptake of health screening. Working collaboratively within a multi-disciplinary team, this will include proactive engagement with the 5 identified National screening programmes. You will be able to communicate effectively with both clinical and non-clinical colleagues to ensure the smooth running of the service. You will be able to communicate effectively with patients and carers and utilise alternative methods of communication whenever this is needed. Consistently demonstrate sensitive communication styles to ensure service users have enough information, in the right format, at the right place and time, to make informed decisions. When required, you will need to be able to communicate difficult, unpleasant, or sensitive information in a way that is supportive and understanding. Act as an advocate when representing patients and colleagues, including engaging and networking with stakeholders. Hold good knowledge of the Mental Capacity Act and the concept and guidance around best interests. Support the validation of learning disability registers held by practices across Devon and access the lists held by local authorities to authenticate the number of health checks completed for people with a learning disability across Devon. Ensure close working relationship with those managing annual health checks, the primary care commissioning and contracting team. Support the delivery of personalised health screening awareness. Undertake community engagement to raise the profile of health screening and screening pathways. Organise and/or run initiatives, including contacting patients, to improve uptake of screening, vaccinations or other services and support the achievement of targets (e.g. under the Quality and Outcomes Framework). Advocacy for health screening across the learning disability population including high levels of preparedness to undertake visits in an individuals own home or residential setting.

Ensure that the Epic system is configured, and/or associated training materials produced, to meet new best practice ways of working, in order to achieve cost-saving benefits and improved workflow processes, whilst working to relevant legal and regulatory frameworks and seeking assistance from the Senior Application Co-ordinator/Analyst or Configuration Manager when required Analyse and document simple to complex clinical and administrative workflows (user requirements), information, data collection and/or reporting requirements and use this information to configure the designated Epic module, and/or to produce the training curriculum and related training materials, to meet these requirements; Analyse and review training progress and variances to define recommendations to maintain schedules and raise any risks or issues highlighted through training to the appropriate level. Investigate SMEs knowledge of application area and workflow and align to the configuration and training design process. Expert and specialist knowledge in the assigned application area and address questions from end users and stakeholders regarding the application.

1. Obtain consent prior to giving care in accordance with Trust policies. 2. Competently undertake delegated duties in line with patient care plans. 3. Ability to use your knowledge and experience to undertake non-routine duties and an understanding to take decisions within your area of responsibility. 4. To carry out a range of (limited) clinical duties with minimal / no supervision, including for example, blood pressure monitoring, oxygen saturation levels, body temperature, pulse rate and respiration rate, glucose monitoring, collection and testing of urine samples / faecal samples / sputum samples and wound swabs ensuring delivery of high-quality patient care at all times. NB: this list is not exhaustive and will vary depending on area of work. 5. Participate in patient assessment providing high quality holistic patient care and escalating concerns about patients to other clinical staff. 6. Practice safe standards of care to patients following Trust guidelines and policies and be able to concentrate for periods throughout the day with occasional interruptions. 7. Provide clinical care in accordance with the infection prevention and health and safety policies and procedures. 8. Maintain the work environment in line with Trust infection control and patient safety policies. 9. Utilising skills to actively facilitate self-care and independence with patients. 10. Promote health education specific to the clinical area and in line with national and local policies. Fr further details please see attached JD&PS.

1. Be recognized as a clinical expert in all aspects of Radiotherapy pathway demonstrating knowledge and practical skills at a senior level maintaining the ability to work as part of the clinical Radiotherapy team delivering safe and accurate CT planning and treatment services 2. Be able to take the clinical lead in providing and delivering highly complex specialised CT planning and treatment techniques and provide support, advice and training for the team. 3. Demonstrate ability to resolve complex clinical issues with problem solving skills and effective autonomous decision-making. 4. Manage the specialist clinical unit workload efficiently according to the needs of the patients, ensuring an efficient smooth running treatment unit 5. To provide effective and safe patient management encompassing all patients needs, using specialist knowledge of treatment side effects, skin reactions and their management. Taking responsibility for referring patients for clinical assessment by a consultant or deputy, prior to commencement of treatment when symptoms become acute. 6. To maintain and continually develop specialist knowledge of ARIA. 7. Provide a supportive and confidential environment for patients, carers and junior staff. 8. To demonstrate effective critical thinking to determine efficacy of treatment referrals, CT requirements, treatment prescriptions, taking appropriate remedial action to mitigate any problems and ensure safe and accurate procedures. 9. Follow departmental procedures but able to use autonomous clinical judgement to make decisions on optimal patient positioning, dose optimization, appropriate imaging techniques and patients condition. 10. Demonstrate high level of skill to enable manipulation and positioning of the patient to achieve accurate set-up Please see the attached job description for full details of roles and responsibilities including personal specification.

Leadership 1. Have an understanding of the clinical research team work-plan and contribute to its achievement. 2. Manage research performance and study timelines of relevant studies. 3. Collaborate with other Trusts and organisations within the region to improve research delivery. 4. Keep up to date with research management issues through liaison with other Research Specialists /Team leaders and link with national networks. 5. Provide relevant supervision and mentorship to members of staff and students. 6. Take responsibility for own health, safety and security and promote the health, safety and security of the wider team. 7. Contribute to the development and implementation of clinical and research policies, procedures and SOPs. 8. Facilitate and maintain effective communication within the research team and between the multidisciplinary clinical team. 9. Assist in the delivery of education and training regarding research for the wider Multidisciplinary Team and act as an ambassador for research. 10. Promote a blame free culture in reporting incidents and where appropriate support local investigation of incidents. 11. Support appropriate studies within PHNT/UHP and its partner organisations as appropriate. Research 1. Be responsible for the delivery of a clinical trial portfolio relevant to the specialty. 2. Ensure that the delivery of studies meet requirements with regards to the Department of Healths Research Governance Framework for Health & Social Care and the EU Clinical Trials Directive by implementing quality systems. 3. Participate in Good Clinical Practice (GCP) training. 4. Contribute to the Expression of Interest / Study Selection process for the relevant specialty. 5. Contribute to study set up, recruitment planning and study delivery. 6. Lead forward and contribute to Patient and Public involvement activities. 7. Be responsible for promoting the appropriate referral and recruitment of patients to clinical research studies. 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. 8. Coordinate and run study visits including off site visits whilst adhering to the lone worker policy. 9. Work with other departments within the Trust to ensure that trial specific investigations and procedures are undertaken as required by the trial protocol, in order to establish eligibility and safety of patients within clinical trials. 10. Contribute to the accurate costing for clinical trials 11. Ensure clear, accurate and concise records are kept for research projects in accordance with all regulatory requirements including the Data Protection Act. 12. Ensure that data is transcribed accurately where required and assist with the maintenance of the Trial Master File. 13. Respond to data queries generated by the study coordinating team within a timely manner. 14. Ensure the recording & reporting of adverse and serious adverse events that occur whilst the participant is in the clinical trial to the trial co-coordinator/Principal Investigator (PI) and R&D office in line with the study protocol, local policies and regulatory requirements. 15. Assess and evaluate the progress of on-going clinical trials for which the post holder has responsibility, maintaining accurate records of the status of studies and providing regular updates to the department on the status of the studies. This will involve ensuring that any Data Management Systems are updated with key trial data and validated efficiently. 16. Escalate on-going study performance issues to the Senior Research Nurse or Team Lead. 17. Co-operate with external and internal audit, data monitoring and quality assurance by working with R&D, sponsors, study monitors and external bodies. 18. Assist in study close down and the preparation of results of research for presentation as posters, abstracts, papers or scientific presentations. Clinical & Professional 1. Be responsible for the care of research participants within the relevant sphere of practice and use opportunities to provide health promotion and patient education. 2. Use relevant clinical knowledge to screen and identify patients suitable for clinical research using inclusion and exclusion criteria and utilising NHS records, screening clinics, visiting wards and outpatients and using Trust IT systems and databases. 3. Act as a resource and role model for all aspects of Research Clinical Practice in order to optimise patient care and clinical practice this may include carrying out physical assessments, conducting sample retrieval and processing, providing or coordinating interventions and treatments, clinical monitoring. 4. Undertake all mandatory training and take part in personal development reviews. 5. Ensure the environment is suitable for patient care and research processes, recognising the importance of privacy, dignity and diversity. 6. Demonstrate professional development and an in-depth knowledge of current clinical and research practice. 7. Provide on-going advice and information to patients and their carers/families with regard to their participation in clinical research in order to facilitate effective informed consent. 8. Where appropriate receive and document written informed consent from research subjects. Training and support for informed consent will be given. 9. Be responsible for the safe and accurate collection of research data through clinical procedures such as venepuncture, history taking, standard observations (height, weight, BP, RR, HR, SpO2 temperature) and other assessments such asECG, physical examinations, disease specific outcome measures, questionnaires, rated scales, qualitative interviewing as required by the protocol. 10. Centrifuge, process track and ship samples in line with protocol requirements. 11. Ensure the safe administration of any treatments and drugs given within the context of a clinical trial. 12. Monitor treatment toxicity/side effects and initiate changes to treatment as required by the protocol. Escalate any concerns to the Principle Investigator or relevant physician. 13. Ensure accurate patient trial documentation, including the use of electronic data capture systems and ensure relevant information is recorded in patients medical notes and case report form in a timely manner. 14. Refer to other specialists as required in order to provide optimal care of the participant. 15. Contribute to the monitoring of clinical standards within the research team. 16. Treat all persons encountered during the course of duties with respect and courtesy and maintain a standard of conduct which best represents the clinical trials team and the Trust. 17. Work within the relevant professional code of conduct (if applicable) demonstrating accountability for own actions and awareness of own limitations. 18. Provide cover for other research nurses/ practitioners as required. 19. Proactively seek feedback from participants and their families during their research involvement. 20. Contribute to Patient and Public Involvement and Engagement activities across the department For further details please see attached JD&PS.

) CLINICAL To be responsible for managing own speech and language therapy caseload of adults with severe learning disabilities with guidance and support from senior colleagues. The degree of communication impairment may range from mild to severe. Managing the caseload includes: Assessment and diagnosis of the communication difficulties of the individual, using both specialist speech and language therapy assessments and also observational and informal assessment skills, in order to form an overall picture of the individuals communication strengths and difficulties, both in understanding and expression, in a variety of situations and settings. Assessment includes the use of video and audio recording where appropriate. The speech and language therapy assessment may contribute to a multi-disciplinary assessment of the individual. In gathering this information there may be conflict of opinion about the individuals communication strengths and needs. The therapist therefore needs to analyse the information given in order to make a judgment about the most appropriate action to take and negotiate this with the people involved. Assessment, diagnosis and management of service users with dysphagia. Clinical supervision provided as appropriate in order to develop skills in dysphagia to a level of independent clinical practice following formal training and clinical supervision until deemed competent. Intervention and/or advice regarding the specific communication difficulties and dysphagia of the individual. Intervention includes; - Specialist speech and language therapy interventions working on the individuals speech and/or language skills. - Using specialist communication programmes including the use of systems designed to be an alternative to, or to augment, speech, including sign and symbols. - The use of specialist programmes such as Intensive Interaction for individuals who have little or no understanding of language. - The setting up and use of microelectronic communication aids. Develops and implements individual and/or group interventions, in collaboration with the service user(s) and MDT to achieve therapeutic goals. Such groups include e.g. communication groups, social skills groups, Makaton etc. Engages service users in therapeutic activities and encourages them in a compassionate manner, to support them in achieving their identified goals. Supervising others who may be implementing the communication programme. Reviewing and evaluating progress, at regular intervals, in order to update the communication programmes as necessary. Discharging as appropriate. To record details of assessment and intervention. To write comprehensive reports giving details of the individuals communication skills and difficulties, and strategies that have been shown to promote more effective communication. To use the appropriate paperwork and electronic recording systems (currently SystmOne) to record contacts and details of assessments, care plans and reviews. To organise group work as required as part of speech and language therapy intervention with people with learning disabilities. To work as part of the core team when a person is being seen by several clinicians from the multi-disciplinary team. The purpose of the core team is to co-ordinate care. This may require negotiation of need and priorities where there is a conflict of opinion. The speech and language therapist may be required to be the lead professional for individuals on their caseload. To develop and deliver training programmes on communication and dysphagia for carers, support staff and professionals involved with people with severe learning disabilities. The training is delivered to groups ranging in size from 2 40 people. To alert the AHP Lead within Livewell Southwest or Service Manager of the Community Learning Disabilities Team where, due to risk or lack of clarity, there is a need for the development of a policy of procedure in order to ensure delivery of a safe and effective speech and language therapy service to people with learning disabilities and to contribute to the development of relevant procedure and policies. To assist others as appropriate, in making information accessible to people with learning disabilities i.e. people who are unable to read and/or have some difficulty in understanding complex language. This assistance may take the form of advice on how to make the materials (it does not necessary mean making materials for other groups of professional). 2) ADMINISTRATIVE 2.1 To keep clear and accurate case notes (normally electronic) and all other necessary records to meet both professional standards, and the standards of the Record Keeping Policy of Livewell Southwest. This is to include input of statistics as required. 2.2 To use word processing programmes, email and the Internet as required. To use specialist software particularly packages using symbols and digital photography to make materials for use as part of an individuals communication programme. 2.3 Prepares therapeutic material such as visual symbol timetables, communication books, symbol cards etc, teaching materials and other speech and language service literature. 2.4 To ensure all equipment and materials used are maintained in good order and inform the budget holder of the need for additional or replacement items. To ensure that all equipment is kept in such a way to meet Health and Safety at Work Regulations. 2.5 To contribute towards making information accessible to individuals with learning disabilities, e.g. leaflets about the service provided etc To advise other agencies on appropriate materials to use on request. 3) PROFFESSIONAL 3.1 To adhere to national and local Standards and Guidelines relating to Professional Practice. 3.2 To be aware of and adhere to current legislation and employers procedures. To attend Mandatory Training as required by the employer. 3.3 To identify own training requirements and update clinical knowledge by engaging in continuing professional development activities including reading appropriate literature, attending local in-service training meetings of speech and language therapists, regional Clinical Excellence Networks and training as appropriate. 3.4 To participate in supervision, personal appraisal and peer review. To take an active part in the speech and language therapy peer clinical supervision group by leading on and contributing to case discussions, review of literature etc. To seek supervision from other members of the LD MDT relating to shared areas of understanding and practice. To receive supervision from the Specialist SLTs who have extensive LD experience. 3.5 To demonstrate ongoing personal development through participation in internal and external development opportunities, reflecting and recording outcomes in a personal log as required for Continuing Professional Development by the RoyalCollege of Speech and Language Therapists and the Health and Care Professions Council. To keep an up to date record of evidence for meeting the criteria set out in the Knowledge and Skills Framework (KSF) for the post. 3.6 To participate in research and/or audit projects as required. To broaden research and audit skills where there is the opportunity to do this.

Person Specification for the post of TAVI training fellowship (Registrar Grade) This post would be suitable for a senior trainee reaching the end of (or completed) sub speciality training in PCI whose aim is to achieve full independence as a TAVI operator The successful candidate must have or be eligible for full GMC registration Essential requirements are good team working, organisation and communication skills Evidence of higher training in cardiology is essential and extensive experience of percutaneous intervention is a requisite On-call commitment Cardiology registrar on-call rota is a 1:11, full shift rota. No requirement to take part on the on-call rota but the post would provide flexibility depending on the appointees training requirements. Education The Fellow is expected to participate in the educational activities of the team, train the more junior members of the PCI/TAVI team and medical students attached to the firm. Research The department has ongoing multi-centre trials and has undertaken original research projects. The Fellow will be expected to spend at least one session a week engaging in research projects with a view to achieve publications and presentations at meetings. Audit The Fellow will be actively involved in audit within the directorate and report on audit projects at the local and regional audit meetings.

Encourage full member participation by presenting an efficient, cheerful, and enthusiastic image at all times. Clean and maintain sport & gym equipment, reporting any faults to the duty manager or supervisor on shift and record them appropriately in book. Be responsible for carrying out weekly maintenance checks of spin bikes, carrying out minor repairs. Conduct gym inductions, programmes, and fitness tests to enable you to advise members how to gain the most from their training and achieve their personal fitness goals. Set up activities for sports users. Plan small fitness challenges and activities for gym members. Assist in the setting up of furniture for activities and functions. Always maintain a visible presence in the fitness suite to coach and advise users where necessary, Take prospective members on a tour of the facility as required. Coach various activities/classes within the centre to ensure members are offered a varied programme. Be familiar with and adhere to the centres health & safety policy together with other centre policies. Collect & return towels etc from the hospital as required. Assist managers with promotional and advertising activities internally and externally. Cover the reception desk when required. Cover classes when appropriate.

Lecturer: To undertake research, professional activities and teaching in line with University/Schools strategy and to carry out leadership, management and engagement activities. Associate Professor: To undertake research in line with Faculty/School research strategy, to deliver high quality research-led and professionally relevant teaching at undergraduate and postgraduate level and to undertake leadership, management and engagement activities. All activities undertaken within these roles will be compliant with the Universitys policies, including Health & Safety, Equality and Diversity, Ethics, Data Protection etc.

Leadership 1. Have an understanding of the clinical research team work-plan and contribute to its achievement. 2. Contribute to research performance of relevant studies. 3. Take responsibility for own health, safety and security. 4. Contribute to the development and implementation of clinical and research policies, procedures and SOPs. 5. Adhere to Standard Operating Procedures without direct supervision. 6. To be able to prioritise workload even when frequently interrupted and under pressure. 7. Maintain effective communication between the research team and patients (who may at times be distressed) tactfully and empathetically. 8. Be part of a blame free culture in reporting incidents and where appropriate support local investigation of incidents. 9. Support appropriate studies within PHNT/UHP and its partner organisations as appropriate. Research 1. Work within the Department of Healths Research Governance Framework for Health & Social Care and the EU Clinical Trials Directive. 2. Participate in Good Clinical Practice (GCP) training. 3. Support the clinical research team by attending study visits and collecting accurate and relevant study data within both the hospital and community setting. 4. Help to ensure that trial specific investigations and procedures are undertaken as required by booking relevant investigations and assisting patients to appointments. 5. Ensure that information is transcribed accurately where required and assist with the maintenance of the Trial Site File. 6. Support external audit and monitoring visits by ordering and collecting patient records and act as a runner or chaperone as required. 7. Collect and handle clinical trial prescriptions and medicinal products. 8. Assist in study close-down procedures. Clinical 1. Assist in the clinical care of research participants in accordance with the specifications of each research study. 2. With training and support, screen and identifying patients suitable for clinical research using inclusion and exclusion criteria and utilising NHS records, screening clinics, visiting wards and outpatients and using Trust IT systems and databases. 3. Undertake clinical activities for which training and competency assessment has been completed. Duties may include performing standard clinical observations (Blood Pressure, Heart Rate, Respiratory Rate, Temperature, Oxygen Saturations, Height and Weight), venepuncture, urine sampling, spirometry, ECG, blood glucose monitoring and physical assessments. 4. With regard to the above clinical duties, assist in the monitoring of treatment toxicity/side effects by reporting any abnormal values to a senior member of the team. 5. Centrifuge, process track and ship samples in line with protocol requirements including handling dry ice following training. 6. Ensure accurate patient trial documentation, including the use of electronic data capture systems and ensure relevant information is recorded in patients medical notes or Case Report Form in a timely manner. 7. Contribute to the monitoring of clinical standards within the research team. 8. Treat all persons encountered during the course of duties with respect and courtesy and maintain a standard of conduct which best represents the clinical trials team and the Trust. 9. Respond quickly and appropriately to enquires and queries, knowing when to escalate issues higher. 10. Demonstrate responsibility for own actions and awareness of own limitations by working within the non- registered practitioners competency framework. 11. Ensure the environment is suitable for patient care and research processes, recognising the importance of privacy, dignity and diversity. 12. Contribute to Patient and Public Involvement and Engagement activities across the department Completing the Local Research competencies Attending all taught days and successfully completing the QCF L5 Diploma for Assistant Practitioners COMMUNICATIONS & WORKING RELATIONSHIPS: Using effective communication techniques to inform and advise others, including discussing sensitive issues; Working collaboratively within the Multi Disciplinary Team, liaising with the following: 1. Patients and their support network 2. Care Cluster Managers 3. Matron 4. Consultants and Doctors 5. Ward Manager / Registered Nurses and all Nursing staff

We are looking for a suitably qualified and experienced individual to provide maternity cover for the role of Training & Communications Manager, starting in May 2024. Key Tasks and Responsibilities of the Post Course Delivery From when the course is published, monitor the bookings, answer queries that may come into the LDC email inbox about the course. Send out delegate lists to trainers for the courses. If there are any cancellations/duplicate bookings on courses, create credit notes on Xero to reimburse the money back to the practice/customer. Send out any resources to delegates around 1-week prior to course delivery date. Send out virtual links/venue details about the course 1-week prior to course date. Ensure that any quizzes/polls that are sent over from the Trainer, are put onto the Zoom session ready before the session starts. Classmarker For Immunisation Foundation courses Trainers will send a quiz that must be completed by all delegates to complete the course. Create class marker on the Classmarker website and send the link created to the Trainer ready for session. Once the Classmarker has been completed compile the quiz score, create certificates and send to delegates. Open virtual sessions on Zoom, let the trainer in and any sponsor (if any). When the course starts, admit all delegates and take attendance on the Excel download of the booking form. Once the course is completed ensure that the attendance is marked on the Live View of Wagtail. General Monitor the LDC email inbox for general day to day queries and answer as applicable. Send out information on courses and/or User Guides. Use Wagtail to ensure that users information is up to date if any queries come in regarding password changes etc. Monitor the main LDC phone daily, taking messages or answering queries. Ensure the phones are diverted if on leave/at meetings etc. Keep a live Request List for any courses that are not yet published and monitor. When courses become available, email delegates to inform them and include booking link. Ensure Request List is updated correctly with person being contacted and what date. Any transfer queries get sent to Education Programme Manager. Social Media Create posts for LinkedIn, Facebook, Instagram and X on Canva. If relevant topics are in news, cross reference these to our courses if possible. Ensure to post on social media at least three times per week. Keep a check on the UK National Days social calendar for any fun or topical events that may be coming up in the year. Create and complete a Newsletter using NewZapp and send out every 2 weeks. Keep a track on the insights of social media to see what is working and what isnt. The role will also involve: Attendance and contribution to team meetings around training provision as required. Development and expansion of training opportunities for General Practice staff. Supporting the development of Learning And Development Centre, including the expansion of our existing training offer into other industries as the company grows. Promote career development and progression to support sustainability and retention in Primary and Community Care. Contribute to the planning and delivery of our Masterclasses Training and Development Assist with the induction of new staff, with regard to departmental policies, procedures and IT Systems. The post-holder will be required to attend training courses, including mandatory courses, which may be identified as part of his/her PDP. Contribute positively to team meetings, bringing relevant issues to the meeting, assisting with the development of the service and assisting with projects identified by the team. To attend regular 1-1 meetings with line manager. Other duties that may reasonably be requested in this post. Maintain your own professional development and update your evidence based practice, knowledge and skills Fulfil all mandatory training requirements for Sentinel Healthcare CIC.

To provide radiographic clinical leadership to research activity within the SW region which includes working with the Academy, imaging network colleagues, Trust staff and the private sector to develop, pilot and introduce software and artificial intelligence products into clinical practice. To be responsible for delivering high quality, effective research and investigations in the field of diagnostic imaging and cancer care, particularly in the development of artificial intelligence, providing and presenting reports and writing articles to the highest professional standards as required. To undertake a lead role in planning, co-coordinating, delivering, developing and evaluating artificial intelligence products in clinical services across the SW region, working with diagnostic imaging staff in multiple sites to deliver improved services to all patients including cancer patients. This is an autonomous and self-directing research role with a requirement to work flexibly to deliver the emerging diagnostic imaging research and AI in imaging agenda. This will include travel to other NHS sites across the region, other regional and national venues requiring either appropriate business car insurance or willingness to travel by public transport. To work with the SW universities and Trusts to develop a comprehensive research development and training offering to all diagnostic imaging and related staff, to be delivered by the SWITA. To proactively promote a culture of learning and the adoption of new technologies across the diagnostic imaging workforce in the SW regions imaging departments. To work collaboratively with health and IT leads across the Trusts as appropriate and promote the role of research and artificial intelligence in diagnostic imaging to all stakeholders. The post holder will also develop strong working relationships with each of the network Trusts research, development and innovation (RD&I) departments to promote and encourage engagement with research across the imaging workforce

Please read the attached Job Description and Person Specification if you have any questions, please do not hesitate to contact us.

To support the Learning and OD team (and Wellbeing team as required) with all necessary administrativeve work as required. Provide line management support, under the direction of the Learning and OD lead to the administrative team, Support with the marketing of Learning and Organisational Development activity using a variety of methods, including email, posters, and social media. Ensuring all the information on offerings for the Learning and Organisational Development is accurate and up to date. Support with engagement and staff feedback activity as required by senior members of the team. Assist with the development of training materials for the team. Support with the facilitation of intervention/courses as required. Ensure there is continuous office and telephone cover across Learning and OD Team and for the Senior Learning and OD and Wellbeing Team. To provide complex information using a variety of communication techniques (i.e. telephone, email, and face to face) to all levels of Trust staff including external agencies and contacts. Organise meetings and manage diaries as directed by the other Senior Leadership team of Learning and OD and Wellbeing. Attend and organise meetings as well as taking minutes as required by the Senior Leadership team of Learning and OD and Wellbeing. Provide general administrative support to the Senior Leadership team of Learning and OD and Wellbeing. To provide administrative support for learning and organisational development interventions/training courses including reporting and monitoring where required. Provide accurate inputting of complex information onto the ESR/OLM/MAPS systems. To support maintaining the Trust Learning Management system and ensure staff bookings are made to the appropriate courses in a timely manner. Carry out administration tasks as appropriate, this includes photocopying, filing, collating information & collating reports. Provide mentoring, in-house training and administrative support to apprentices as required. Assist in the management of all the organisational development team EPROC orders, stationery, invoicing, stock control, ordering and onsite equipment issues. Update SharePoint to ensure all departmental information is accurate and engaging to our internal customers. Create slide decks, format reports, and manage action logs as required. Support with recruitment activity for the Senior team and department, using the TRAC system. For further details please see attached JD&PS.