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Clinical Trial Manager (CTM) – 6-Month Contract Location: London, UK (Hybrid) A global leader in rare genetic disease therapeutics is seeking an experienced Clinical Trial Manager (CTM) to join their Global Study Operations team on a 6-month contract. This role is responsible for the end-to-end management and delivery of clinical studies, ensuring timelines, quality, and budget targets are consistently met. About the Role: As a Clinical Trial Manager (CTM), you will take ownership of clinical study execution across Phase 1 through post-approval. You will lead cross-functional teams, oversee vendors, and ensure studies are delivered on time, within budget, and in compliance with regulatory requirements. This is a highly visible role with direct impact on advancing innovative therapies for rare diseases. What You’ll Do: • Lead global clinical trial execution from study start-up through close-out, • Oversee CROs and external vendors to ensure performance, quality, and delivery, • Drive study timelines, budgets, and risk management strategies, • Ensure compliance with GCP, regulatory requirements, and internal SOPs, • Lead study team meetings and act as the primary point of contact for study operations, • Oversee site management, monitoring strategy, and issue resolution, • Review and approve key study documents (protocols, plans, reports), • Ensure accurate and timely maintenance of Trial Master Files (TMF), • Partner cross-functionally with Clinical, Regulatory, Data Management, and Safety teams, • Provide operational leadership and escalation management as needed Who You Are: • A confident study leader with strong project management capabilities, • Proactive, solutions-oriented, and able to manage complexity, • Experienced in global clinical trial delivery and vendor oversight, • Strong communicator with the ability to influence cross-functional stakeholders, • Detail-oriented while maintaining a strategic, big-picture perspective Qualifications: • BSc or higher in nursing, life sciences, or related field (or equivalent experience), • Significant experience in clinical trial management within pharma/biotech, • Proven experience managing CROs and external vendors, • Strong knowledge of drug development processes and regulatory requirements (GCP, ICH), • Experience across multiple study phases preferred Ready to help transform rare disease care? Apply now to play a key role in delivering life-changing therapies to patients worldwide.

About the Company We're working with an innovative clinical-stage biotechnology company developing next-generation precision medicines for serious diseases with significant unmet need. Leveraging advanced platform technologies and a highly collaborative scientific approach, the company is advancing a growing pipeline of early clinical and translational programmes. Following recent progression into clinical development, the organisation is entering an exciting phase of growth and is expanding its operational capabilities to support ongoing and future clinical studies globally. The company offers a fast-paced, collaborative, and science-driven environment with the opportunity to work across cutting-edge therapeutic programmes alongside experienced industry leaders. The Opportunity We are seeking an experienced and highly organised Clinical Project Manager to support the delivery of early-phase clinical programmes across a growing pipeline. This individual will play a central role in the operational management and cross-functional coordination of Phase 1/2 clinical studies, working closely with internal teams, CROs, vendors, and external partners to ensure high-quality and timely execution of clinical development activities. The ideal candidate will bring strong operational oversight experience within biotech or CRO environments, alongside the ability to operate effectively within a lean and fast-moving organisation. Key Responsibilities Clinical Trial Delivery & Oversight • Support the planning, execution, and oversight of Phase 1/2 clinical studies across multiple programmes, • Manage day-to-day operational activities in collaboration with CROs, vendors, and study teams, • Track study timelines, milestones, risks, and deliverables to ensure successful study execution, • Support oversight of site activation, patient recruitment, study conduct, and close-out activities, • Ensure studies are conducted in compliance with protocol, GCP, SOPs, and regulatory requirements CRO & Vendor Management • Act as a key operational contact for CROs and external vendors, • Monitor vendor performance, timelines, quality metrics, and study deliverables, • Support issue escalation, risk mitigation, and resolution of operational challenges, • Facilitate effective communication and coordination across external partners Cross-Functional Project Coordination • Coordinate activities across Clinical Operations, Clinical Development, Regulatory, Translational Medicine, Biomarkers, Data Management, Biostatistics, Safety, and CMC teams, • Support preparation and maintenance of study plans, governance materials, and project trackers, • Facilitate study team meetings and ensure clear documentation of actions and decisions, • Maintain visibility across programme timelines, dependencies, and critical path activities Reporting & Governance • Prepare operational updates, study status reports, and risk assessments for internal leadership, • Support inspection readiness and maintenance of audit-ready documentation, • Contribute to development and continuous improvement of operational processes and systems, • Ensure accurate maintenance of trial management documentation and study records Strategic & Operational Support • Contribute to building scalable clinical operations infrastructure within a growing biotech environment, • Support study start-up planning for future pipeline programmes, • Assist with feasibility assessments, study planning, and operational strategy discussions Must Haves: • Early-phase biotech experience, • Experience supporting global or multi-regional clinical studies, • Proven experience managing or coordinating clinical trials within biotech, pharma, or CRO environments, • Strong understanding of Phase 1/2 clinical trial operations, • Experience overseeing CROs and external vendors, • Ability to manage multiple stakeholders and cross-functional workstreams, • Excellent organisational, communication, and project management skills, • Experience operating within fast-paced or resource-constrained environments, • Strong understanding of GCP and clinical development processes Skills & Competencies • Strong attention to detail and execution focus, • Proactive and solutions-oriented mindset, • Comfortable operating across scientific and operational teams, • Strong communication and stakeholder management abilities, • Ability to prioritise effectively within a dynamic environment, • Collaborative and team-oriented approach

🚀 Clinical Trial Manager (Contract) | Cell Therapy / Oncology | UK Hybrid We are seeking an experienced Clinical Trial Manager to join a leading biotechnology organisation on a 12-month contract basis. 📍 Location: Stockley Park, UK (Hybrid – 3 days onsite per week required) This is an exciting opportunity to play a key role in the delivery of innovative Cell Therapy and Oncology clinical trials, managing European and potentially global study activities across Phase I–III programmes. Key Responsibilities ✅ Manage the European component of global outsourced clinical studies ✅ Oversee CROs and external vendors to ensure successful study delivery ✅ Maintain study timelines, budgets, and operational plans ✅ Coordinate the review and development of study documentation including protocols, informed consent forms, monitoring plans, investigator brochures, and clinical study reports ✅ Collaborate with cross-functional teams to drive study progress and resolve operational challenges ✅ Support vendor selection activities, including RFP development and evaluation ✅ Conduct oversight monitoring visits where required ✅ Ensure effective management of site budgets and contracts ✅ Contribute to clinical operations initiatives and continuous improvement activities What We're Looking For 🔹 Strong clinical trial management experience within multinational studies (preferably across Europe) 🔹 Experience in Oncology and/or Cell Therapy highly preferred 🔹 Previous monitoring experience is highly desirable 🔹 Solid understanding of ICH-GCP guidelines and FDA/EU clinical trial regulations 🔹 Excellent stakeholder management, communication, and organisational skills 🔹 Ability to manage multiple priorities in a fast-paced environment 🔹 Experience working with CROs and external vendors Why Apply? This role offers the opportunity to work on cutting-edge therapies that have the potential to transform patient outcomes, while collaborating with highly experienced global teams in a supportive and dynamic environment. ✈️ Some international travel may be required. Interested or know someone who could be a great fit? Get in touch to learn more.

Senior Clinical Trial Manager – Global Digital Health Programme Location: London, UK Working pattern: On-site 5 days per week, London Bridge. The Opportunity This is an opportunity to join a large-scale, globally recognised research programme delivering clinical trials at significant international scale. You would be part of a multi-partner initiative involving leading healthcare organisations, technology partners, and research institutions, focused on improving maternal and early childhood health outcomes through innovative, data-driven approaches. The programme operates across multiple countries and sites, requiring strong coordination, operational oversight, and consistent delivery of high-quality clinical trials. The Role As Senior Clinical Trial Manager, you will take ownership of the operational delivery of clinical trials across the programme. You will be responsible for ensuring trials are run to the highest standards, maintaining compliance with regulatory requirements, Good Clinical Practice, and data integrity expectations across all participating sites. You will work closely with senior stakeholders, including the Chief Investigator and Programme leadership, acting as a central point of coordination across research teams, sites, and partners. Key Responsibilities • Lead day-to-day management of clinical trials, including site selection, initiation, and monitoring, • Act as the primary point of contact for research teams, trial sites, and external partners, • Develop, maintain, and manage the Trial Master File and all associated documentation, • Ensure all trial activities align with protocol, regulatory requirements, and GCP standards, • Plan and monitor participant recruitment, identifying and addressing any barriers, • Coordinate trial supplies and ensure compliance with intervention protocols, • Monitor data quality in collaboration with statisticians and data managers, • Schedule and support Trial Management Group, Steering Committee, and Data Monitoring Committee meetings, • Prepare and submit regulatory and ethics documentation, including amendments and progress reports, • Manage communication with sponsor organisations and ensure all contractual documentation is in place, • Oversee financial aspects of trials, including forecasting and budget tracking, • Develop and implement procedures to support trial delivery, • Supervise and support junior staff where applicable What You’ll Bring • Degree in a relevant health or scientific discipline, with postgraduate training in research methods, • Strong experience in clinical trial management within a research or clinical environment, • Solid understanding of Good Clinical Practice and regulatory frameworks, • Experience working with clinical systems such as CTMS and electronic data capture platforms, • Strong organisational and problem-solving skills, with the ability to manage complex trial operations, • Experience managing risk within clinical trials and implementing mitigation strategies, • Confidence working across multiple stakeholders in a multi-site environment, • Strong communication skills and ability to coordinate across teams Nice to Have • Formal qualification in clinical trials or project management, • Experience within digital, remote, or large-scale international trials, • Understanding of AI-enabled or technology-driven research environments, • Experience with financial planning and oversight in clinical trials, • Previous experience supervising or mentoring team members Why This Role • Work on a global programme delivering high-impact clinical research, • Exposure to complex, multi-site international trials, • Collaborate with leading clinicians, researchers, and programme leaders, • Be part of a well-funded, long-term initiative with strong backing and clear direction, • Opportunity to take ownership of trial delivery in a large, structured programme If you are an experienced clinical trial professional looking to step into a role with scale, impact, and operational responsibility, this is a strong opportunity to do so.

We're Hiring: Associate Clinical Trial Manager (Part-Time | 12-Month Contract) We are seeking an experienced Associate Clinical Trial Manager or a Senior Clinical Trial Associate to join our team on a part-time, 12-month contract. This role will support the operational delivery of innovative clinical studies across Oncology and Cell Therapy, working closely with cross-functional teams, sites, and vendors to ensure studies are conducted efficiently and in compliance with applicable regulations and GCP requirements. The ideal candidate will have clinical research experience, strong organizational skills, and a passion for advancing cutting-edge therapies that make a difference to patients. 📍 Location: North West London ⏳ Contract: Part-Time | 12 Months 🔬 Therapeutic Areas: Oncology & Cell Therapy If interested please send your CV ASAP and I'll be in touch!!

Temporary Life Science Administrator\n\nOur client is a well-established pharmaceutical organisation who enhance and improve the health of millions of people every day and are looking for help with a project.\n\nThis is a significant role supporting an important project, where you will be migrating sequences from one application to another. You will need to address any sequences that present challenges, which will necessitate technical knowledge that will be provided through training. Attention to detail is crucial, as you will be handling a high volume of data in Excel spreadsheets. Additionally, you should possess strong communication skills, as you will be interacting with both external and internal stakeholders via email.\n\nThis role would be an ideal step for a Life Science graduate who is looking to make a transition into an administration role. The successful candidate will have a relevant Life Science background and degree with a strong knowledge of Microsoft Excel.\n\nHybrid working (8 days per month in the Office)\nOffice based in Canary Wharf\n£14.20ph\n37 hours per week (Monday to Friday)\n6 months temporary\nASAP startAn amazing benefits package includes:\n\nWeekly pay every Friday\nEasy timesheet accessibility with mobile support\nUp to 29 days annual leave\nPerks at work and discount schemes for all major retailers and over 150 high street stores\nAccess to free eye-care vouchers and discounts towards glasses for VDU purposes\nAccess to well-being platforms\nFREE access to online LinkedIn Learning courses, there are 1000's of courses and videos available to enhance your learning and skillset, everything from Microsoft systems to soft skills such as delivering great Customer Service\nTemp of the Month awards\nDedicated consultant to support your job search and offer expert interview tipsDuties of the role:\n\nManage the agency database(s) and check consistency between public registers\nInputting applications on the Agency databases and supporting the application specialists with allocation of both clinical trials applications and monitoring of timelines\nAssists with generating performance measures for UK trial, and trial registration and summary results posting\nWork with the application specialists in data analysis, presentation of Unit metrics for reports and enquiries as required\nAssist the Business Support Manager and Operations Lead in implementing Internal Quality Measures and Scientific Advice Meetings\nAssist the Senior Safety Manager with finance aspects of new fees from clinical trial annual safety reportsOffice Angels is an employment agency and business. We are an equal-opportunities employer who puts expertise, energy and enthusiasm into improving everyone's chance of being part of the workplace. We respect and appreciate people of all ethnicities, generations, religious beliefs, sexual orientations, gender identities, abilities and more. By showcasing talents, skills and unique experiences in an inclusive environment, we help individuals thrive. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.\n\nOffice Angels acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. Office Angels UK is an Equal Opportunities Employer.\n\nBy applying for this role your details will be submitted to Office Angels. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website

At Mural Health, our mission is to make clinical trials easier for participants and caregivers by eliminating barriers to participation. As a Customer Success Manager (CSM), you’ll ensure our customers achieve meaningful outcomes while also helping Mural Health refine and scale how we deliver value. You’ll serve as a trusted advisor to clinical trial sponsors and sites, guiding them to maximize the value of our platform and strengthening their ability to support participants. You’ll proactively contribute your expertise and insights to strengthen operations while collaborating closely with cross-functional teams to make a meaningful impact. Reports to: Director of Customer Success in the US Location: UK- Remote What You’ll Do • Champion customers: Serve as the primary post-sale partner, building trusted, strategic relationships that deliver measurable impact from onboarding through full life cycle of each study, • Enable adoption & outcomes: Lead onboarding and training, monitor account health, and deliver regular business reviews that highlight results, insights, and opportunities, • Take Initiative: Take ownership of complex accounts, anticipate challenges, and drive solutions, • Bring insights to scale: Identify process improvements, strengthen internal workflows, and influence customer success strategy, • Collaborate cross-functionally: Advocate for customers across Mural Health, partnering with product, operations, Patient Kindness, and marketing teams to improve solutions and participant support, • Drive growth: Identify and support additional opportunities, collaborating with sales and marketing to expand customer relationships, • Share the story: Capture and communicate customer feedback, case studies, and success stories to drive internal improvements and customer advocacy, • You are an exceptional communicator: clear, persuasive, and effective with stakeholders at every level, • You are a problem solver: able to structure problems, create actionable strategies, and influence stakeholders, • You thrive in a startup environment: adaptable, proactive, and comfortable managing ambiguity, • You combine strategic vision and tactical execution: delivering on customer needs today while shaping long-term improvements, • You are motivated to improve patient and caregiver experiences in clinical trials, • 3-5+ years of progressive client-facing experience in Account Management, Customer Success, or Consulting, leading customer engagements and initiatives, • Bachelor's degree in business, life sciences, healthcare, or related field or equivalent work experience., • Experience in healthcare, life sciences, or clinical trials with understanding of pharmaceutical/biotech sponsor relationships preferred, • Proven track record managing complex customer accounts and delivering measurable outcomes (retention, adoption, satisfaction, or process improvements), • Experience influencing change and driving improvements across product, operations, or data-driven teams., • Excellent communication and presentation skills with ability to engage both clinical and technical audiences, • Strong problem-solving abilities and customer-centric mindset, • Experience with CRM and project management systems (Salesforce, Asana, Jira, Aha!, or similar), • A sense of humor! Mural Health is proud to provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. We also provide reasonable accommodations to individuals with disabilities in accordance with applicable laws. If you require reasonable accommodation to complete a job application, pre-employment testing, a job interview or to otherwise participate in the hiring process, or for your role at Mural Health, please contact careers@muralhealth.com. If you’d like more information about your EEO rights as an applicant, please visit the US Department of Labor's website.

Medpace is seeking an Associate Clinical Trial Manager (aCTM) in London to join their Clinical Trial Management team. This full-time position is ideal for recent PhD graduates in Life Sciences looking to enter the industry with a focus on clinical project management.

Job Summary Medpace is the leading CRO for Biotech companies and is continuing to add a Director of Clinical Trial Management (Operational role) to join our Clinical Trial Management Group in London, UK. Clinical Trial Managers with expertise in Oncology or other therapy areas are welcome to continu

As a Clinical Trial Manager (CTM), you will take ownership of clinical study execution across Phase 1 through post-approval. Clinical Trial Manager (CTM) – 6-Month Contract. A global leader in rare genetic disease therapeutics is seeking an experienced Clinical Trial Manager (CTM) to join their Gl

Business Development Manager Revolutionary SaaS | Electronic Health Records | Clinical Trials & Drug Development Salary: £50,000–£60,000 (negotiable) + uncapped commission + excellent benefits Location: Home-based with access to Manchester offices (1–2 days per month) The Opportunity This is not just another sales role. You’ll be joining a fast-growing UK business at the forefront of transforming how life-saving drugs are developed. With a proven track record of securing multi-million-pound transatlantic deals with leading global pharmaceutical companies, the business is scaling rapidly—and you could be a key part of that journey. If you’re looking to sell a genuinely innovative solution, work with an exceptional leadership team, and accelerate your career in a high-growth environment, this is your chance. About the Company & Solution This organisation is redefining how Electronic Health Record (EHR) data is used in clinical research. Their cutting-edge SaaS platform analyses and interprets real-world healthcare data, turning it into powerful insights that drive smarter, faster drug development. Clients—including major global pharmaceutical companies—use this platform to: • Access real-time, searchable patient data, • Optimise clinical trial design and execution, • Reduce development timelines and costs, • Bring life-saving treatments to market faster The impact? Tangible improvements in global health outcomes, powered by data. The Role As a Business Development Manager, you will play a pivotal role in driving new business growth across the pharmaceutical and CRO landscape. This is a strategic, consultative sales position where you’ll engage senior stakeholders and build demand for a complex, high-value solution. You’ll thrive here if you enjoy creating opportunities from scratch, navigating long sales cycles, and influencing decision-makers in a highly specialised market. Key Responsibilities • Build, manage, and convert a high-quality pipeline of new business opportunities, • Identify and engage key stakeholders across pharmaceutical companies and CROs, • Develop relationships with teams in clinical development, medical affairs, and real-world evidence, • Lead consultative sales processes from initial engagement through to close, • Articulate the value of a complex, data-driven SaaS solution, • Maintain accurate pipeline visibility and forecasting via CRM About You We’re looking for a driven, commercially minded sales professional who is ready to step up and make an impact. You will have: • 1–3 years’ experience in a relevant sales or business development role, • Exposure to the life sciences, pharmaceutical, or CRO market, • A track record of generating new business and hitting targets, • Experience selling solutions (ideally SaaS or data-driven offerings), • The ability to engage multiple stakeholders and manage complex sales cycles, • A proactive, self-starting mindset with the hunger to succeed Most importantly, you’re ambitious, resilient, and excited by the opportunity to sell something that genuinely makes a difference. Why Join? • Sell a truly innovative, market-leading solution, • Be part of a company closing multi-million-pound global deals, • Work directly with an experienced and supportive leadership team, • Enjoy significant earning potential with uncapped commission, • Accelerate your career in a high-growth, high-impact sector, • Contribute to advancements in life-saving drug development

We'll look to you to create a safe and supportive environment for residents with range of physical and mental needs, whilst also relying on your professional judgement to make critical clinical decisions. You'll need to have current NMC registration and a good knowledge of the most up-to-date clinic

If you'd like to use your clinical and people skills in an organisation that provides the quality care you'd expect for your loved ones, this is a rewarding and empowering place to be. We'll look to you to create a safe and supportive environment for residents with range of physical and mental needs

Registered Nurse Days - Hendon, London.Bring your unique skills to our caring, supportive team, when you join Signature Senior Lifestyle as a Registered Nurse.Whether you are experienced or newly qualified, you'll enjoy several opportunities to grow and develop your nursing career at our luxury care

Strong knowledge of up-to-date clinical practices. Clear pathways for career progression into specialist clinical or digital care roles. You'll support residents and patients with a wide range of physical, psychological, and social needs, ensuring they receive the dignity, respect, and clinical exce

Registered Nurse (Day Shifts) - Kingston Upon Thames, London.Bring your unique skills to our caring, supportive team, when you join Signature Senior Lifestyle as a Registered Nurse.Whether you are experienced or newly qualified, you'll enjoy several opportunities to grow and develop your nursing car

A national charity is looking for a Contracts Manager to join their team on a remote basis. Advising Operations Manager on outputs and improvement areas.

To join us as a Care Home Deputy Manager you'll need experience in helping residents with different health needs and a successful track record of managing safeguarding investigations and clinical risk assessments. As Care Home Deputy Manager of a Barchester care home, you'll support the delivery of

To join us as Home Manager you will have inspirational leadership skills with a passion for person centred care, with a successful track record of developing and motivating teams to deliver outstanding personalised care through continuous improvement. Barchester can offer long term career growth and

Every client receives dedicated attention from their own Operations Manager and Registered Nurse, ensuring continuity, compassion, and the highest standards of care in their preferred environment.

Du erreichst beständig Deine Ziele und entwickelst Dich rasch zum Senior Sales Manager weiter.

Become a Self-Employed Delivery Driver with Evri and Start Earning This Summer.Looking to boost your income over the summer months? Whether you're saving for a holiday, covering extra expenses, or just want more cash in your pocket, now’s the perfect time to get started.Join Evri as a self-employe

Become a Self-Employed Delivery Driver with Evri and Start Earning This Summer.Looking to boost your income over the summer months? Whether you're saving for a holiday, covering extra expenses, or just want more cash in your pocket, now’s the perfect time to get started.Join Evri as a self-employe

Key Account Manager, Aesthetics, London 💉. Proven experience selling within medical aesthetics injectables or a closely aligned clinical sales environment. Established credibility with aesthetic practitioners, injectors and clinic owners, able to influence both clinical and commercial decisions.

Become a Self-Employed Delivery Driver with Evri and Start Earning This Summer.Looking to boost your income over the summer months? Whether you're saving for a holiday, covering extra expenses, or just want more cash in your pocket, now’s the perfect time to get started.Join Evri as a self-employe

Partnerships and Philanthropy Manager (Home based, International Environmental Charity). This is an excellent opportunity for an ambitious Partnerships and Philanthropy Manager to play a key role in driving income growth through trusts and foundations, philanthropy and selected corporate partnership

Vacancy Service Delivery Driver – Class C Location: Hartshill Business: The ReFood AD plants operate as integrated recycling units, processing a variety of food wastes to produce biogas, renewable electricity, heat and ReGrow (a nutrient-rich fertiliser for local farms).The plants also recycle t

Role Description Female Support Worker Make Every Day Matter! Location: Surbiton, Surrey Salary: £13.Driving Licence: Manual UK licence preferrable Visa Sponsorships: Not available Make a Real Difference Are you looking for a role where your patience, consistency and care genuinely improve so

We are looking for passionate Childrens Support Workers who are available to work on a flexible basis.As a Childrens Support Worker you will work as part of a team to deliver a high standard of care at all times and support the Young Persons emotional wellbeing.You recognise that the role is to help

Become a Self-Employed Delivery Driver with Evri and Start Earning This Summer.Looking to boost your income over the summer months? Whether youre saving for a holiday, covering extra expenses, or just want more cash in your pocket, nows the perfect time to get started.Join Evri as a self-employed de

Children's Home Registered Manager. We are seeking an experienced and committed xrnqpay Registered Manager to lead our new solo children's home in.

We are seeking a passionate and energetic Home Manager to join our vibrant and dedicated team at The Terrace.

Interaction recruitment is hiring HGV Class 1 Drivers in Marston Gate for a fantastic temp to perm position We're looking for energetic, enthusiastic individuals with a can-do attitude to work as a HGV 1 Driver.You will be delivering to unmanned stores keys & instructions given daily.A FLT licence w

Registered Clinician accreted to use NHS Pathways Clinical Decision Support Software. Leading clinical quality improvement through insight, collaboration and targeted development to enhance performance and patient care. Lead and support Clinical Quality Improvement (CQI) processes, using audit, data

We are looking for a passionate.As a Senior you will lead a team of support workers to deliver a high standard of care at all times.You recognise that the role is to help support service users maximise their choices, rights and decisions.The successful candidate must have;.NVQ Level 3 in Residential

If you love working in care but want more balance and control over your working week, Peters Dean Care offers the flexibility youve been looking for.We offer flexible Support Worker roles that allow you to do meaningful work you care about, while still working regular hours every week.Youll work acr

Work collaboratively with the Manager and team to uphold the home's values and approach.