77 Clinical Assistant jobs in the United Kingdom
Optometric Clinical Assistant - International BTEC Standards Verifier
Posted 10 days ago
Job Viewed
Job Description
**Optometric Clinical Assistant**
**About Pearson**
At Pearson we're committed to a world that's always learning. From bringing lectures vividly to life to turning textbooks into laptop lessons, we are always re-examining the way people learn best. We are bold thinkers and standout innovators who motivate each other to explore new frontiers in an environment that supports and inspires us to be better. By pushing the boundaries of technology, and each other to surpass these boundaries, we create seeds of learning that become the catalyst for the world's innovations, personal and global.
We are the UK's largest awarding body and offer qualifications that are globally recognised and benchmarked, with educational excellence rooted in a range of General and Vocational courses.
**Purpose**
The Standards Verifier plays a key role in maintaining the integrity and consistency of vocational qualifications by ensuring that assessment and internal verification practices meet national standards. This involves providing expert subject-specific support to centres, conducting sampling and verification activities, delivering clear and constructive feedback, and contributing to the ongoing development of quality assurance processes. Through regular training, collaboration with internal teams, and engagement with centres, the Standards Verifier helps uphold Pearson's commitment to high-quality, reliable assessment.
**Core Services**
When carrying out your role; please be mindful that you represent Pearson and that you should always maintain your professional integrity. Therefore, it is essential that you:
Ensure compliance with all parts of the terms and conditions and other policies.
Act at all times in a way which will not bring Pearson, it's employees and its representatives into disrepute.
Adhere to Pearson policies and guidance related to data privacy and security of information.
Remain respectful and advocate for others to ensure diversity, equity, and inclusion, in a professional manner.
Raise any concerns if you suspect or are made away of any malpractice, maladministration and/ or Safeguarding issues.
Adhere to deadlines given by Pearson and ensure that all work is carried out to the best of an individual's ability.
Respect the confidentiality of centres and learners.
You are responsible for the provision of your own IT equipment and must therefore ensure it is capable of running Pearson required software, relevant malware, appropriate anti-virus software and a suitable internet connection. As well as this we require a Personal email address attached to a secure account. (This cannot be a work email)
Collaborate and communicate in a timely manner with Pearson.
**Role Specific Services and Expectations**
In addition to Pearson's core service expectations, this role requires the following specialised responsibilities:
Stay up to date with relevant qualification specifications and, where applicable, National Occupational Standards.
Provide expert advice, guidance, and support tailored to your subject area and in line with verification requirements.
Attend and complete all mandatory training and annual standardisation activities within required timelines.
Conduct centre visits as required for qualifications involving visiting verification, following guidance from the Assessment team and subject to approval.
Adhere to Pearson's quality assurance processes and follow prescribed sampling strategies for allocated qualifications.
Review learner work and internal verification records to ensure accuracy and compliance.
Ensure assessment decisions are valid, consistent, and aligned with national standards.
Provide constructive feedback and support to centres during the sampling process.
Produce comprehensive and actionable sampling reports for each centre visited.
Clearly communicate when standards are not met and outline the necessary corrective actions.
Assist centres in addressing issues, implementing improvements, and maintaining ongoing compliance.
Identify and recommend suitable learner work or assessment materials for use in future training and standardisation events.
Maintain regular communication with your Pearson supervisor and work collaboratively with internal teams.
This role requires a proactive approach to quality assurance and a commitment to maintaining Pearson's high standards across all responsibilities.
**Experience and Qualifications required:**
**Experience:**
As a representative of the company, you will be expected to have experience in, or be able to demonstrate the ability of the following:
Strong background in quality assurance and assessment practices.
Experience in verifying regulated qualifications.
Exceptional communication skills.
Proven ability to deliver and coordinate training sessions, including standardisation and other standards-focused activities.
In-depth knowledge of specifications relevant to your specialist sector, encompassing both internal.
Examples of previous leadership or support roles in essential quality assurance activities.
**Qualifications:**
Qualifications required to apply for your chosen role at Pearson will depend on the qualification you are delivering. Please contact Pearson ahead of your application if you have any questions on the requirements.
**Vocational Qualifications (eg. BTEC)**
A minimum of one full academic year of teaching experience in the relevant subject area/sector within the last 8 years and/or extensive knowledge and experience in Pearson assessment, quality and processes and national standards within the last 5 years
Relevant CPD evidence in the subject area/sector within the last 12 months
Hold a relevant qualification in the subject area/sector.
A UK recognised teaching qualification
Please note upon successful application Pearson may ask you to provide proof of the qualifications required.
**Application Information**
We have a number of opportunities available for teaching professionals to join our growing teams of examiners, moderators and verifiers.
#LI-KB1
Clinical Project Assistant
Posted 1 day ago
Job Viewed
Job Description
PE Global is recruiting a Clinical Project Associate to support an AI-enabled Clinical Design Lab within a leading global pharmaceutical company. This initiative is part of a strategic effort to integrate artificial intelligence into clinical trial design and development processes.
The successful candidate will provide project management and cross-functional coordination support to ensure timely delivery of key milestones across multiple teams, including clinical, data science, digital, and operational functions. The role is an initial 12-month contract and the rate for this role is £200-400/day Umbrella based on experience.
Key Responsibilities
- Support the planning, tracking, and delivery of activities within the AI-enabled Clinical Design Lab.
- Maintain and update detailed project timelines, milestones, and deliverables.
- Coordinate cross-functional collaboration between clinical, data science, and technology teams.
- Assist in identifying and managing project risks, issues, and dependencies; support mitigation planning.
- Prepare and maintain project documentation, including agendas, meeting minutes, and action logs.
- Assist with report and presentation preparation (e.g., PowerPoint summaries for senior stakeholders).
- Facilitate communication across internal stakeholders to ensure project alignment and visibility.
- Support change management and adoption activities related to AI and digital initiatives in clinical development.
- Monitor project performance metrics, ensuring data accuracy and quality in deliverables.
- Contribute to continuous improvement efforts and knowledge sharing within the Clinical Design Lab.
Requirements
- Bachelor’s degree in Life Sciences, Public Health, or a related field.
- 2–3 years of experience in project coordination or project management within the pharmaceutical or life sciences industry.
- Demonstrated experience working cross-functionally across clinical, data, and/or digital teams.
- Solid understanding of the drug development and clinical trial process.
- Strong organizational and time management skills with the ability to manage multiple priorities.
- Proficiency in Microsoft Office (Excel, Word, PowerPoint) and project tracking tools.
- Excellent communication and interpersonal skills, with proven stakeholder management experience.
- Detail-oriented, proactive, and comfortable working both independently and collaboratively.
Desirable:
- Experience supporting AI, digital, or data-driven initiatives in clinical or R&D settings.
- Familiarity with change management or digital transformation projects.
- Understanding of agile project management principles.
Please note PE Global cannot assist with visa sponsorship. Candidates must have the full right to live and work in the UK for at least the next 12 months.
Clinical Project Assistant
Posted 1 day ago
Job Viewed
Job Description
PE Global is recruiting a Clinical Project Associate to support an AI-enabled Clinical Design Lab within a leading global pharmaceutical company. This initiative is part of a strategic effort to integrate artificial intelligence into clinical trial design and development processes.
The successful candidate will provide project management and cross-functional coordination support to ensure timely delivery of key milestones across multiple teams, including clinical, data science, digital, and operational functions. The role is an initial 12-month contract and the rate for this role is £200-400/day Umbrella based on experience.
Key Responsibilities
- Support the planning, tracking, and delivery of activities within the AI-enabled Clinical Design Lab.
- Maintain and update detailed project timelines, milestones, and deliverables.
- Coordinate cross-functional collaboration between clinical, data science, and technology teams.
- Assist in identifying and managing project risks, issues, and dependencies; support mitigation planning.
- Prepare and maintain project documentation, including agendas, meeting minutes, and action logs.
- Assist with report and presentation preparation (e.g., PowerPoint summaries for senior stakeholders).
- Facilitate communication across internal stakeholders to ensure project alignment and visibility.
- Support change management and adoption activities related to AI and digital initiatives in clinical development.
- Monitor project performance metrics, ensuring data accuracy and quality in deliverables.
- Contribute to continuous improvement efforts and knowledge sharing within the Clinical Design Lab.
Requirements
- Bachelor’s degree in Life Sciences, Public Health, or a related field.
- 2–3 years of experience in project coordination or project management within the pharmaceutical or life sciences industry.
- Demonstrated experience working cross-functionally across clinical, data, and/or digital teams.
- Solid understanding of the drug development and clinical trial process.
- Strong organizational and time management skills with the ability to manage multiple priorities.
- Proficiency in Microsoft Office (Excel, Word, PowerPoint) and project tracking tools.
- Excellent communication and interpersonal skills, with proven stakeholder management experience.
- Detail-oriented, proactive, and comfortable working both independently and collaboratively.
Desirable:
- Experience supporting AI, digital, or data-driven initiatives in clinical or R&D settings.
- Familiarity with change management or digital transformation projects.
- Understanding of agile project management principles.
Please note PE Global cannot assist with visa sponsorship. Candidates must have the full right to live and work in the UK for at least the next 12 months.
Clinical Project Assistant
Posted today
Job Viewed
Job Description
PE Global is recruiting a Clinical Project Assistant for our pharmaceutical client based in London. The role is an initial 12-month contract and the rate for this role is £200-400/day Umbrella based on experience.
Key Responsibilities:
- Maintain and update project timelines and deliverables
- Track project progress and report on key milestones
- Organize and maintain project documentation, including meeting agendas and minutes
- Schedule and help facilitate team meetings and workshops
- Assist with the preparation of reports and presentations (e.g., PowerPoint)
- Communicate with internal teams and stakeholders to ensure alignment
- Monitor deliverables for accuracy and quality
- Identify project risks and support mitigation planning
- Analyse data related to project performance and industry practices
Requirements:
- Bachelor's degree in Life Sciences, Public Health, or related field
- 2–3 years of experience in clinical research, project coordination, or consulting
- Basic understanding of drug development and clinical trial processes
- Strong organizational and time management skills
- Ability to manage multiple tasks and deadlines
- Proficient in Microsoft Office (Excel, Word, PowerPoint) and project tracking tools
- Excellent written and verbal communication skills in English
- Comfortable working independently and as part of a team
- Attention to detail and a methodical approach to tasks
- Desirable:
Experience with AI tools in clinical development
Please note PE Global cannot assist with visa sponsorship. Candidates will need the full right to live and work within the UK for at least the next 12 months.
Clinical Trial Assistant
Posted 2 days ago
Job Viewed
Job Description
(This is role is requires frequent travel to Luton)
IQVIA is a leading global provider of contract research services, advanced analytics and technology solutions to the life sciences industry formed through the merger of IMS Health and Quintiles.
Take your therapeutic expertise to the next level and help drive the evolution of clinical development for a variety of sponsors.
As a Clinical Trial Assistant within our full-service model, you'll have the opportunity to embrace your passion for a specific therapeutic area and work with cutting-edge technology developed specifically for CTAs.
With access to world-class training and professional development, we'll give you the tools you need to create the career you want.
Do you want to know more about IQVIA? then see what Forbes said about us!
Functions of a Clinical Trial Assistant (CTA)**
+ Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.
+ Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for completeness.
+ Assist CRAs/iCRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
+ Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
+ Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
+ May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval.
+ May perform assigned administrative tasks to support team members with clinical trial execution.
**Required Knowledge and Skills**
+ Awareness of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Knowledge of applicable protocol requirements as provided in company training
+ Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint
+ Good written and verbal communication skills including excellent command of English
+ Effective time management and organizational skills
+ Ability to establish and maintain effective working relationships with coworkers, managers and clients
*Please note - this role is not eligible for UK visa sponsorship*
_IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential._
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
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Clinical Project Assistant
Posted today
Job Viewed
Job Description
PE Global is recruiting a Clinical Project Associate to support an AI-enabled Clinical Design Lab within a leading global pharmaceutical company. This initiative is part of a strategic effort to integrate artificial intelligence into clinical trial design and development processes.
The successful candidate will provide project management and cross-functional coordination support to ensure timely delivery of key milestones across multiple teams, including clinical, data science, digital, and operational functions. The role is an initial 12-month contract and the rate for this role is £200-400/day Umbrella based on experience.
Key Responsibilities
- Support the planning, tracking, and delivery of activities within the AI-enabled Clinical Design Lab.
- Maintain and update detailed project timelines, milestones, and deliverables.
- Coordinate cross-functional collaboration between clinical, data science, and technology teams.
- Assist in identifying and managing project risks, issues, and dependencies; support mitigation planning.
- Prepare and maintain project documentation, including agendas, meeting minutes, and action logs.
- Assist with report and presentation preparation (e.g., PowerPoint summaries for senior stakeholders).
- Facilitate communication across internal stakeholders to ensure project alignment and visibility.
- Support change management and adoption activities related to AI and digital initiatives in clinical development.
- Monitor project performance metrics, ensuring data accuracy and quality in deliverables.
- Contribute to continuous improvement efforts and knowledge sharing within the Clinical Design Lab.
Requirements
- Bachelor’s degree in Life Sciences, Public Health, or a related field.
- 2–3 years of experience in project coordination or project management within the pharmaceutical or life sciences industry.
- Demonstrated experience working cross-functionally across clinical, data, and/or digital teams.
- Solid understanding of the drug development and clinical trial process.
- Strong organizational and time management skills with the ability to manage multiple priorities.
- Proficiency in Microsoft Office (Excel, Word, PowerPoint) and project tracking tools.
- Excellent communication and interpersonal skills, with proven stakeholder management experience.
- Detail-oriented, proactive, and comfortable working both independently and collaboratively.
Desirable:
- Experience supporting AI, digital, or data-driven initiatives in clinical or R&D settings.
- Familiarity with change management or digital transformation projects.
- Understanding of agile project management principles.
Please note PE Global cannot assist with visa sponsorship. Candidates must have the full right to live and work in the UK for at least the next 12 months.
Clinical Project Assistant
Posted today
Job Viewed
Job Description
PE Global is recruiting a Clinical Project Associate to support an AI-enabled Clinical Design Lab within a leading global pharmaceutical company. This initiative is part of a strategic effort to integrate artificial intelligence into clinical trial design and development processes.
The successful candidate will provide project management and cross-functional coordination support to ensure timely delivery of key milestones across multiple teams, including clinical, data science, digital, and operational functions. The role is an initial 12-month contract and the rate for this role is £200-400/day Umbrella based on experience.
Key Responsibilities
- Support the planning, tracking, and delivery of activities within the AI-enabled Clinical Design Lab.
- Maintain and update detailed project timelines, milestones, and deliverables.
- Coordinate cross-functional collaboration between clinical, data science, and technology teams.
- Assist in identifying and managing project risks, issues, and dependencies; support mitigation planning.
- Prepare and maintain project documentation, including agendas, meeting minutes, and action logs.
- Assist with report and presentation preparation (e.g., PowerPoint summaries for senior stakeholders).
- Facilitate communication across internal stakeholders to ensure project alignment and visibility.
- Support change management and adoption activities related to AI and digital initiatives in clinical development.
- Monitor project performance metrics, ensuring data accuracy and quality in deliverables.
- Contribute to continuous improvement efforts and knowledge sharing within the Clinical Design Lab.
Requirements
- Bachelor’s degree in Life Sciences, Public Health, or a related field.
- 2–3 years of experience in project coordination or project management within the pharmaceutical or life sciences industry.
- Demonstrated experience working cross-functionally across clinical, data, and/or digital teams.
- Solid understanding of the drug development and clinical trial process.
- Strong organizational and time management skills with the ability to manage multiple priorities.
- Proficiency in Microsoft Office (Excel, Word, PowerPoint) and project tracking tools.
- Excellent communication and interpersonal skills, with proven stakeholder management experience.
- Detail-oriented, proactive, and comfortable working both independently and collaboratively.
Desirable:
- Experience supporting AI, digital, or data-driven initiatives in clinical or R&D settings.
- Familiarity with change management or digital transformation projects.
- Understanding of agile project management principles.
Please note PE Global cannot assist with visa sponsorship. Candidates must have the full right to live and work in the UK for at least the next 12 months.
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Clinical Support Worker
Posted today
Job Viewed
Job Description
Petra Matewa, Team Leader or
About The Role
Here at the Mid Yorkshire Trust an exciting opportunity has arisen for a Radiology Clinical Support Worker to become a key role within the Magnetic Resonance Imaging (MRI) department here in Radiology. We require someone who has excellent organisational and Interpersonal skills and who can continuously improve themselves and help others to do so within our department.
The successful candidate will be able to demonstrate good team membership skills, have the ability to act diplomatically in sensitive situations involving patients or staff, be punctual, understand the need for patient confidentiality, and be able to follow instructions accurately.
We are a four site trust - Pinderfields Hospital Wakefield, Pontefract Hospital, Dewsbury & District Hospital, and the new Wakefield Community Diagnostic Centre in the Westgate Retail Park.
As part of your role you will be required to work across all four sites on a rota basis covering long days, weekends and bank holidays.
The Mid Yorkshire Trust has excellent travel links to Leeds, Sheffield, Doncaster and Bradford. We are close to both the M1 and the M62.
If you would like to attend for an informal chat or a look round, please contact a MRI Team Leader on extension or
Main duties
To work as a member of the team delivering a high-quality MRI service within Radiology.
The service comprises scanners located in Pinderfields Hospital, Wakefield; Dewsbury & District Hospital; Pontefract General Infirmary and the new Wakefield Community Diagnostic Centre.
To carry out administration duties in a manner that supports departmental targets and ensures compliance with standard operating procedures.
To undertake administrative and patient care duties to enable a patient focussed service. The post holder is required to rotate across administrative and patient care functions.
The postholder is required to keep confidential all information and documentation relating to either a patient, a member of staff or service business, which he/she comes into contact with. All staff are expected to respect the requirements of the Data Protection Act 1998, as this incorporates the need for a high standard of data quality, confidentiality and information security.
Key Requirements
- Maintain a professional appearance in line with the Trust dress code.
- Uphold the Trust's values and behaviours (available on the Trust web site) and behave in a manner fitting with the responsible position of the role, maintaining the public confidence.
- Maintain professional and courteous working relationships with staff and respect the equality and diversity of each and every person he/she comes into contact with-in the course of his/her business
- Uphold the privacy and dignity of the client group and respect equality at all times.
- The post holder will maintain a smart appearance and adhere to the uniform policy particularly in relation to jewellery and footwear.
- The post holder will deal professionally and courteously with colleagues, patients, and visitors.
- The post holder will adhere to the Trust's policy relating to confidentiality.
- The post holder will undertake an annual appraisal.
Clinical
- To assist the Radiologist, Radiographers, and other staff in providing a comprehensive efficient service.
- To prepare and administer to patients, oral preparation, under guidance of the Radiographers and in compliance with departmental working practise.
- The post holder will adhere to moving and handling policies to ensure that patients come to no harm.
- The post holder will ensure that patients are appropriately dressed for their procedure and assist the patient in dressing and undressing as required.
- The post holder will help position the patient as appropriate to the procedure to be undertaken.
- The post holder will undertake observation of patients recording observations within the patient records and reporting concerns to the Radiographers or medical staff as appropriate.
- To assist in patient care, for example to act as a chaperone and to provide care/comfort as required.
- To assist, if required, radiographic and nursing colleagues when undertaking interventional procedures.
- The post holder will help prepare the room for the patient's examination including filling the automatic injector under supervision.
- The post holder will adhere to control of infection policies in support of patients with known infection.
- The post holder will ensure that the environment and equipment is fit for purpose in order to reduce the incidence of hospital acquired infection.
- The post holder will undergo training for intravenous access and assist in the administration of contrast agents where appropriate.
- Maintain patient privacy and dignity at all times.
- Support the service to deliver the best possible patient experience.
- Core working hours will include long days, weekend and bank holiday working.
- PLEASE SEE ATTACHED JOB DESCRIPTION AND PERSON SPECIFICATION FOR MORE INFORMATION**
Be part of MY team
We are an acute trust caring for over one million people in Wakefield and Kirklees. Our 10,000 staff work in patients' homes, the community, and our three hospitals in Pontefract, Dewsbury, and Pinderfields (Wakefield). We prioritise our people and values so we can deliver the best possible care to patients. Our team is friendly, passionate, and innovative, always seeking better ways to work.
We support work-life balance and foster a diverse, inclusive environment where everyone belongs. Our staff networks offer safe spaces to share ideas and concerns so we can increase awareness and appreciation of equality, diversity, and inclusion. We welcome applicants from all backgrounds and especially encourage members of the LGBTQ+ community, ethnic minority groups, and people with disabilities or neurodivergence to apply, as they are currently underrepresented in the Trust.
If you value caring, high standards, improvement, and respect, join the MY team to make a difference every day.
Application Guidance
We understand that more applicants are using AI technology to help with their applications. While these tools can be useful, they cannot fully capture your skills, knowledge, and experience. It's important that you personalise your application. Relying solely on AI is not recommended, as it may reduce your chances of success. Our screening process is thorough, so if you have used AI, please make sure to disclose this on your application form.
Our Benefits
- Access to the NHS pension plan
- Generous holiday allowance of 27 days plus bank holidays, increasing with 5 and 10 years of service
- Exceptional employee health and wellbeing services
- Extensive benefits and support, including:
- Onsite nurseries and childcare salary sacrifice scheme
- Cycle to work scheme
- Home electronics scheme
- Car lease salary sacrifice scheme
- Working carers support and advice, carers network and carers passport
- Flexible working options and family and carer-friendly policies
- Established staff networks, including LGBTQ+ and Race Equality
- Career progression, training and support
Skilled worker sponsorship
You can find out more about skilled worker and health and care visas on our .
Clinical Support Worker
Posted today
Job Viewed
Job Description
We are looking for a proactive, positive, respectful, supportive, reliable and trustworthy person to join our team of Clinical Support Workers on the Aston Unit at Congleton War Memorial Hospital.
If you are enthusiastic and dedicated to delivering high quality care to our patients, we want to hear from you.
The role exists to provide a multi- skilled worker who, under the supervision of who under of a Registered Nurse, supports the Multidisciplinary Team with clinical and nonclinical practices on order to provide excellent patient centred care.
You will be required to successfully complete the Care Certificate within 3 months of starting the post.
The position is predominantly nights but on occasions you may be requested to work days.
Hours per week: 37.5
Work as part of a ward based team, assist in the delivery of a high standard of nursing care, acting in a professional manner at all times. Provide support to the Registered Nurse and other team members by observing and reporting aspects of patient care as appropriate and to promptly alert the registered nurse to any issues or risks. Be able to communicate in a manner that is understood and always in a polite and respectful manner. Maintain effective communication with the multi disciplinary team and ensure documentation is maintained within the post holders sphere of competence.
Promote equality for all individuals, to include promoting anti-discriminatory practice, supporting individual rights and choice within service delivery. Enable patients to meet their personal hygiene and toileting needs in accordance with individual preferences and clinical need. Maintaining patients' comfort, privacy & dignity at all times. Assist in providing adequate nutrition and hydration for patients based on their individual needs as directed by the multi-disciplinary team. Promoting patients mobility as appropriate and assist in the movement and transfer of patients, using manual handling aids as appropriate to maximise the safety of staff and patients, in accordance with the patients' individual care plan.
Maintain patients skin integrity based on individual need using appropriate resources, reporting findings to a Registered Nurse.
We are committed to providing the best quality integrated care to our patients. To achieve this aim we need highly motivated staff who are united by common values and behaviours.
We believe our workforce is our greatest asset and we actively support our staff to develop their capabilities to the full, with a variety of learning and development opportunities.
Whether you are just starting out in your career or are looking to use your skills and experience in a new role, East Cheshire NHS Trust is the right employer for you. We look forward to you joining us so that we can bring out your best.
Please be aware that this post requires an Enhanced with Barred list Disclosure and Barring Service (DBS) check, the cost of which is payable by the successful candidate. If you have lived or worked abroad for 6 months or more in the last 5 years you will need to obtain an overseas police clearance. Further information can be found on the additional information links at the bottom of the advert.
Please read the attached Applicant Pack prior to completing your application form to find out more information.
Please download a copy of the Job Description and Person Specification located under the Supporting documents heading to read more about the advertised role.
As part of making your application we encourage you to review the Trusts Careers webpage Careers :: East Cheshire NHS Trust for more information about working for East Cheshire NHS Trust.
We are an equal opportunities employer and welcome all applications irrespective of age, disability, gender, sexual orientation, race or religion. The Trust is a Disability Confident Leader and as such, applicants with disabilities will be offered an interview providing they meet the minimum criteria for the post (outlined in the Person Specification).
Applicants are advised to apply early as we reserve the right to close the advert prior to the advertised closing date should we receive a large number of applications.
We look forward to receiving your application.
Overseas candidates wishing to apply who would require sponsorship can determine the likelihood of obtaining a CoS for the post by assessing their circumstances against criteria specified on the Visas and immigration - GOV.UK )
Clinical Support Manager
Posted 24 days ago
Job Viewed
Job Description
Responsibilities:
- Manage and lead a team of care coordinators, support workers, and other healthcare professionals.
- Develop, implement, and review personalised care plans for individuals, ensuring they meet specific needs and preferences.
- Oversee the day-to-day operations of care services, including scheduling, resource allocation, and service delivery.
- Conduct regular assessments of client needs and the effectiveness of care provision.
- Ensure all care activities comply with regulatory requirements, CQC standards, and company policies.
- Provide training, supervision, and professional development opportunities for care staff.
- Handle client and family concerns, complaints, and feedback effectively and empathetically.
- Liaise with external agencies, healthcare professionals, and local authorities to ensure integrated care.
- Maintain accurate and confidential client records and documentation.
- Promote a culture of dignity, respect, and independence for all individuals receiving care.
- Participate in on-call rotas as required and respond to emergency situations.
- Contribute to the strategic development and continuous improvement of care services.
- Manage budgets and resources efficiently to ensure service sustainability.
- Uphold the highest ethical standards in all aspects of service delivery.
- Diploma in Health and Social Care (Level 5) or equivalent qualification.
- Significant experience in a management or supervisory role within the social care or healthcare sector.
- In-depth knowledge of relevant legislation and standards governing social care (e.g., CQC).
- Proven ability to lead, motivate, and manage a diverse team.
- Excellent communication, interpersonal, and problem-solving skills.
- Strong organisational and time-management abilities.
- Proficiency in IT, including care management software.
- A genuine passion for providing high-quality, person-centred care.
- Ability to work effectively under pressure and make sound decisions.
- A full UK driving licence may be required for some aspects of the role.