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Our client is a highly successful British technology company renowned for designing innovative computing platforms used by millions of developers, educators, engineers, and hobbyists worldwide. With a strong focus on accessible and high-performance computing, the company has established itself as a global leader in embedded and edge computing technologies. As they continue to invest in the development of next-generation silicon platforms, they are expanding their in-house ASIC capability to support an exciting product roadmap. This role would suit someone who enjoys working autonomously with like minded people. They have an excellent leadership team and working culture. The Opportunity As a Verification Engineer, you will take ownership for IP and chip level verification planning and execution, and will be constantly interacting with the design team, composing detailed verification plans and creating test benches from scratch or using shared verification components. Requirements Hands-on experience with at least three projects Experience of creating test benches from scratch, using Systemverilog, Python, or UVM Experience of writing embedded C, ideally for Cortex M-class MCUs Good technical understanding in at least one complex IP protocol,e.g. PCIe, HDMI, USB, SDIO, AMBA bus architectures Ability to write functional coverage and SVA Good understanding of design/front-end processes Experience with low-power simulations SoC verification concepts: memory caches, DMA, security architecture (TrustZone or equivalent). Experience of Cadence simulation tool flow including gate-level simulation. Scripting languages: Bash, TCL, Make, YAML, etc. Please note that this role is based in Cambridge and requires full-time onsite attendance. This opportunity offers a fantastic compensation package and a number of non-monetary benefits. This is a great opportunity to join them as they leap into their next growth phase. For more information, please contact Rachel Mason at IC Resources

Job Description Summary#LI-HybridPosition Location: Cambridge, MA We are Clinical Sciences and Innovation at Novartis. A dynamic group of Clinical Trial Leaders (Clinical Scientists) who plan and execute early phase trials worldwide. From First-in-Human to ph2a studies and beyond. We design and operationalize trials, ensuring they run smoothly, on time and – most importantly – with patients’ interests to the fore.Curious, unbossed and inspired; we are committed to flexibility in the workplace.As a member of our team, you will support or lead the clinical science and operations of planning and executing translational medicine clinical trials. Collaborate across our global network. Partner with outstanding physicians and scientists. Build therapeutic area expertise. Revolutionize next-generation, digital and patient-centric trial design. Be always curious, innovative and inspiring.Job DescriptionKey Responsibilities:Operationally and scientifically lead complex clinical studiesDrive and deliver aspects of global clinical trial execution from study design, set-up and recruitment to final reportingLead the matrix-management of robust global clinical trial teams, collaborating across the organization and externally with service providers/investigator sitesDrive the development of clinical study protocols, clinical operations execution plans and other required documentsEnsure quality conduct and document standards are applied across the clinical trial lifecycleLead clinical data reviewContribute to project/program level plansMay mentor junior team membersSupport optimization of standard methodologies in clinical trial operations and adopt an open learning and sharing environmentUnleash the value of data and digital within clinical studies Ultimately, YOU will help bring new technologies and therapies closer to our patientsEssential Requirements:Bachelors in life science/healthcare required; Advanced degree or equivalent education/degree in life sciences/ healthcare preferred (PhD/MD/ PharmD/ Masters)6+ years’ experience in clinical trials developmentA broad knowledge of the drug development field; preferably within the pharma industry.Strong project management experience; excellent planning, prioritization and organizational skills; used to managing multiple priorities concurrentlyDemonstrates high learning agility in therapeutic areaDesirable Requirements:Experience in study design and protocol development/writing is highly desirableThe salary for this position is expected to range between $126,000 and $234,000 per year.The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.To learn more about the culture, rewards and benefits we offer our people click here.EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.Salary Range$126,000.00 - $234,000.00Skills DesiredBudget Management, Clinical Research, Clinical Trials, Coaching, Data Analysis, Data Integrity, Learning Design, Risk MonitoringSummaryLocation: Cambridge (USA)Type: Full time

Job Description Summary#LI-HybridLocation: CambridgeInternal Title: Senior Principal Scientist or Associate DirectorThe Biomarker Development (BMD) group at the Novartis is seeking a Senior Principal Scientist or Associate Director to join our Clinical Imaging and Analytics team and provide strategic, scientific, technical and operational leadership on the optimal use of imaging in drug development. Be part of an imaging department with deep expertise in structural, molecular, and quantitative biomarkers and their application in translation and development. The successful candidate will provide scientific leadership across Oncology (including Radioligand Imaging), Neuroscience, Cardiovascular/Renal/Metabolic, and emerging precision medicine initiatives, including xRNA programs and novel tracer development. You will partner with clinical trial teams to establish the role of imaging endpoints along novel biological mechanisms across diverse therapeutic areas. The role offers a wide view of programs across various stages as they transition from research to early development, and subsequently to PhII/III trials. As a part of building imaging endpoints, the role also provides unique exposure to variety of other critical biomarkers (soluble and genetics) for an integrated view of identifying unique patient populations, assess target engagement and generate decision-critical readouts of efficacy, safety and mechanism of action.Job DescriptionKey Responibilities:Act as an internal expert in molecular and clinical imaging, including PET, SPECT and other advanced imaging methodologies relevant to clinical and translational drug development. Partner with Oncology and General Medicine teams to develop and lead fit-for-purpose imaging strategies across research, early development and late-stage clinical development. Develop imaging biomarker, target engagement and translational imaging strategies that generate decision-critical evidence for patient selection, pharmacodynamics, efficacy, safety and mechanism of action. Collaborate with internal operational teams, imaging CROs, academic centers and external experts to design, execute and interpret imaging readouts across multisite clinical trials. Ensure quality and timely execution of imaging trials to deliver critical drug development decisions; be agile and responsive to clinical teams during the course of design, execution and interpretation of imaging trials.Evaluate and implement novel imaging techniques, quantitative methodologies, AI-enabled analytics and imaging platform capabilities, to improve portfolio decision making.Essential Requirements:PhD or MD or MD/PhD with 8+ years of experience in PET/SPECT Imaging in academia or industry, including at least 5 years supporting clinical drug development.Deep technical expertise in PET and/or SPECT as applied to clinical drug developmentStrong understanding of clinical trial design, endpoint development, biomarker strategy, statistical considerations and clinical data flow is required. Experience with clinical protocol writing across line functions is required. Experience with PET/SPECT tracer development, radioligand imaging, dosimetry, receptor occupancy or clinical Radioligand/Radiopharmaceutical Therapy (RLT/RPT) is a plus. Experience in regulatory interactions, submissions, first-in-human imaging studies, endpoint validation or qualification is a plus.Understanding of sites, budgets, imaging CROs, imaging data standards and experience with multisite trial execution is a plus.Demonstrated track record of innovative research preferably across imaging modalitiesProactive, self-motivated and independent working style; comfortable operating in a multidisciplinary and highly matrixed organization. Ability to drive for results with urgency, accountability and sound judgment while balancing scientific quality and portfolio priorities.Strong communication skills in English, with demonstrated ability to influence, mentor and act as a collaborative servant leader.This is a dual level posting. The final level & title of the offer role would be determined by the hiring team based on the skills, experience & capabilities required to perform the role at the level the role has been offered.The salary for this position is expected to range between:Senior Principal Scientist: $132,300 and $245,700 per year.Associate Director: $145,600 and $270,400 per year.The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.To learn more about the culture, rewards and benefits we offer our people click here.EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.Salary Range$132,300.00 - $245,700.00Skills DesiredAnalytical Thinking, Chemical Biology, Chemistry, Clinical Research, Clinical Trials, Collaboration, Curious Mindset, Data Analysis, Decision Making, Detail-Oriented, Drug Development, Ethics, Machine Learning (ML), Medical Research, Mentorship, Patient Care, Science, Stakeholder Engagement, Stakeholder ManagementSummaryLocation: Cambridge (USA)Type: Full time

27th July, 2026You will play a key role in designing, executing, and maintaining test across both manual and automated test frameworks on new and legacy Platforms. You will also work closely with Development, Conformance, and Business Support teams to enhance product quality and efficiency. Come and join Sepura Ltd at an exciting time of growth and progress your career within this innovative technology company, based in Waterbeach, Cambridge.Day to Day: Our customer base includes many different industries and markets around the world. Our complete TETRA and LTE solutions have been developed specifically for users in multiple sectors to face their critical communications challenges. There is no such thing as a typical day here at Sepura. You will be supported by your manager and team, as well as collaborating with other departments across the business. The activities you will be responsible for include:Writing and executing functional, regression, system, and performance testing to ensure product compliance with industry standards.Testing of software solutions / applications to ensure that the developed products meet the requirements and are free of defects.Reading and understanding requirements documentation provided by a Product Definition Team, Product Strategy Team or External test houseInvolved in test planning, test execution, defect tracking, and reporting to stakeholders.Producing and maintaining appropriate documentation for tracking quality metricsDevelop and execute manual and automated test cases for Sepura’s LTE and TETRA products.Collaborate with software, hardware, and system engineers to identify defects, reproduce issues, and drive resolutions.Ensure test environments, test equipment, and infrastructure are maintained and available for testing.Participate in design and requirements reviews to provide testability feedback.Mentor junior test engineers and contribute to the growth of the test team. This job involves some travelling so the successful applicant will have a full, clean driving licence, own car, and valid passport. Travel expenses will be paid.This role may require Security Clearance in the future. What you need to succeed:Qualifications & Certifications:Bachelor’s or Master’s degree in computer science, Electronics, Telecommunications, or a related field.3 years UK residency is required for security checkISTQB certification (preferred but not mandatory).Experience and Skills:A high level of communication skills and technical understanding5+ years of experience in manual and automation testing, preferably in embedded systems, telecommunications, or mission-critical applications.Experience with manual testing methodologies for embedded software and hardware products.Familiarity with TETRA and LTE technologies is highly desirable.Excellent problem-solving skills, attention to detail, and ability to work in an agile environment.A critical eye for detail and capable of delivering critical feedback without damaging relationships.Technical Skills:Knowledge of protocol testing, RF testing, and communication interfaces (e.g., TCP/IP, UDP, Serial, Bluetooth, etc.) is a plus.Strong experience in using Test Management tools (e.g., JIRA, TestRail,Jama).Hands-on experience with testing frameworks and tools (e.g., Selenium, JUnit, TestNG, Cypress, Postman, JMeter).Understanding of APIs and backend testing.

We have an opportunity for an experienced Senior System Engineer to work for our global client based in Cambourne, Cambridgeshire. Our clients’ Technology Solutions division is evolving. They are moving to a Product Operating Model – a new way of working that empowers product teams to take full ownership and accountability for delivering customer and business value in ways customers love and that work for the business. \n Our client’s product and platform teams are cross-functional and durable, bringing together all the skills required to deliver impactful outcomes. Each team includes a Product Manager, Technology Lead, Product Designer, Delivery Lead, engineers, and developers. \n Our client believes in customer centricity, ownership, and accountability. Solutions must be: \n\n • Valuable – customers choose to buy or use them\n, • Viable – aligned with business constraints and goals\n, • Usable – intuitive and user-friendly\n, • Feasible – achievable with our technical capabilities\n\n Leadership of the Product team is shared between the Product Manager and the Technology Lead, ensuring balanced guidance that bridges product vision and technical execution. \n As Senior System Engineer you will have significant impact on our multi-disciplinary R&D projects, grow with us as we venture into new technologies and will lead work groups in our projects as part of the connected devices line of products during the product lifecycle of both discovery and delivery. \n This role is a temporary contract position for 2 years. You will be required to work 37.5 hours per week and our client offers hybrid working (minimum 2 days onsite and the rest working remotely from home). The role offers a generous hourly rate of £ per hour depending on experience, plus 25 days holiday pro rata. \n Role Functions \n The responsibilities will include defining System, HW, Embedded, ATE, SW & Integration requirements as well as contributing to the design stage of each discipline, defining the protocol, technical problem solving, proof of concept and field testing and assisting in tests design and investigations. Management of manufacturing automating projects to ensure the efforts satisfy business requirements. Responsibilities will encompass all phases of a project life-cycle including concept requirement, design, testing, installation, qualification and training. Is considered expert with many years of experience and may be a non-management level lead of a team. \n Experience, Skills and Knowledge \n The position requires multidisciplinary understanding, ability to quickly grasp new technological aspects as well as constraints , the capability to work in a multi-site matrix organization and working closely in a Product and Platform team with other system engineers, embedded software developers, HW engineers, Integration Engineers as well as backend and front-end teams. As well as: \n\n • Ability to focus on what's important.\n, • Organized and able to work well in a structured process environment\n, • Strong desire for learning and innovation.\n, • “hands-on” approach.\n, • Excellent team player.\n, • Good verbal & written communication Skills.\n\n Qualifications & Education \n Requirements \n\n • BSC/MSc in Electrical engineering or higher\n, • Minimum of 5 years of experience in system engineering of multidisciplinary systems\n, • Experience in working with communication products, Embedded, HW, RF systems\n, • Problem solver with good personal and teamwork skills.\n, • Ability to understand complex IoT systems and quickly grasp new technical concepts with focus on challenges ahead and alternative comparison\n, • Experience of working in complex multidisciplinary projects that requires a high level of technical know-how\n, • Demonstrated application of S88, S95, automation scope principles, competitive decision making, and MMD IT architecture standards for optimal business outcomes.\n\n Advantage \n\n • Experience with Linux environment\n, • Experience in working with Atlassian suite and/or Azure DevOps\n, • Experience with Agentic AI for discovery and innovation\n, • Coding capabilities (C/C#/Java/Python)\n, • Experience with RF communication technologies (BLE, WiFi, LTE-M, LoRa, etc)\n, • Knowledge in backend systems and serverless solutions\n, • Working with Cloud based infrastructure for IoT devices\n\n Due to the high volume of applications we receive, only shortlisted candidates will be contacted. If you do not hear from us, please assume your application has not been successful on this occasion. We appreciate your interest and wish you the best of luck in your job search. \n

Job Description SummaryPosition Location: Cambridge, MA #LI-hybrid*This role is based in Cambridge, MA. Please only apply if this location is accessible for you.Welcome to where we thrive together! Are you ready to join a community where you can make a real impact on the world through your exceptional communication skills? At Novartis, we believe in creating a positive and inclusive work environment where we can solve the toughest healthcare challenges together.The Strategic Feasibility Expert is accountable for the clinical feasibility strategy for Biomedical Research (BR) therapeutic areas (TAs) and patient trials managed by Translational Medicine (TM). The Strategic Feasibility Expert is a TA-aligned, single point-of-contact to ensure study timelines and enrolment plans reflect indication footprint and site landscaping enabling successful trial execution. The Strategic Feasibility Expert will lead early medical and operational feasibility, proactively identify high quality academic and commercial sites, and engage early with key strategic investigators, sites and networksJob DescriptionKey responsibilities:Leads the strategic identification, selection of countries and sites for a given Therapeutic Area and individual clinical trials.Provides early, strategic feasibility input (including early medical and operational feasibility) for a given therapeutic area (TA), indication, or study, through the utilization of relevant tools, databases, and historical metrics.Accountable within the Clinical Trial Team (CTT) for appropriate site identification and anticipating and relaying hurdles/delays for consideration in ultimate selection and timelines.Consolidates feasibility feedback and potential site list for CTT decision making. May act as the point of escalation when a site selection or sourcing challenge is identified which can impact the trial timelines.Engages internally and externally to identify new investigators /sites. Maintains knowledge of investigators /sites mapping in alignment with TA /indication strategy.Maintains awareness of site performance data e.g. recruitment.Identifies and maintains relationships with key strategic investigators, sites, and networks for a given indication, program, or TA. Identifies and establishes strategic partnerships as appropriate.Works closely with the CTT during protocol development to understand site specifications and to provide robust input into the study operational plan.Works closely with the Clinical Finance Manager (CFM) on the early strategic planning and to provide input to site budget, timelines, and TTG impact.Works closely with key global stakeholders, including Therapeutic Area (TA) Heads, Clinical Scientists, Translational Medicine Experts (TMEs), Country Organizations (CO), Global Clinical Operations (GCO).Essential Requirements:At least 8 to 10 years’ experience in pharmaceutical industry /biotech /CRO drug development environmentExcellent understanding of drug development process, early clinical development preferred.Superior knowledge of clinical trials site selection, global /country specific requirements, timelines and challenges in clinical trial execution processDemonstrated ability to work effectively in a global, matrix organization and build strong positive relationships.Ability to work independently with demonstrated willingness to make decisions and to take responsibility for such.Desirable Requirements:Advanced computer literacy.Excellent organizational skills. Ability to adjust to multiple demands, shifting priorities and unexpected events while maintaining a positive work attitude.The salary for this position is expected to range between $152,600 to $283,400 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.To learn more about the culture, rewards and benefits we offer our people click here.EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.Salary Range$152,600.00 - $283,400.00Skills DesiredBudget Management, Clinical Research, Clinical Trial Protocols, Clinical Trials, Coaching, Cross-Functional Teamwork, Data Analysis, Learning Design, Lifesciences (Inactive), Risk Management, Risk MonitoringSummaryLocation: Cambridge (USA)Type: Full time

\n Job Title: Director of Pathology Location: Cambridge, UK Hybrid working: Minimum 3 days per week in the office Introduction to role:\n Are you ready to bring decisive medical leadership in pathology to accelerate personalised diagnostics that guide clinical trials and patient care? This is a chance to shape how novel biomarkers become trusted tests that identify the right patients for the right therapies, faster. \n You will join our internal accredited laboratory delivering in-house diagnostic testing for early-phase clinical studies and pioneering approaches in patient stratification. Your oversight will ensure assays are robust, validated and clinically meaningful, directly influencing how our medicines are developed and how patients are selected for studies. Working at the intersection of pathology, quality, and translational science, you will help advance companion and complementary diagnostics— including computational pathology and image analysis—across a biomarker-driven portfolio. \n At Director level, you will look beyond daily operations to set direction, influence governance, and represent the laboratory in internal and external forums. Will you help us lift diagnostic standards, bring new technologies into practice, and translate cutting-edge science into results that clinicians and patients can trust? Accountabilities:\n \n • Medical and Technical Oversight: Provide pathology oversight of assay performance, result review and reporting practices in an accredited environment supporting clinical and biomarker development.\n, • CAP/CLIA and GxP Compliance: Act in a role aligned to CAP/CLIA expectations; ensure testing and reporting practices meet regulatory and professional standards, including ISO 15189, GCP, IVDR and HTA requirements.\n, • Result Authorisation and Interpretation: Review, interpret and approve laboratory results and reports, ensuring outputs are scientifically valid, clinically appropriate and compliant with defined quality requirements; contribute to clinical and scientific interpretation of pathology and biomarker data.\n, • Method Evaluation and Approval: As technical lead, evaluate and approve novel test methods; ensure fitness for purpose and appropriate validation or verification before clinical use.\n, • Operational Partnership: Work closely with the Laboratory Director, QA/QC and operational leadership to evolve methods, procedures, instrumentation, staffing models and workflow design.\n, • Strategy and Companion Diagnostics: Provide scientific and medical input into assay and biomarker strategy, including companion diagnostic development and clinical implementation planning; align with broader clinical development objectives.\n, • Innovation and Digital Pathology: Drive continuous improvement and the introduction of emerging technologies, including digital pathology, image analysis and data-enabled diagnostic workflows.\n, • Clinical Trial Support: Provide medical and technical oversight for prospective patient testing in clinical studies, ensuring protocol-aligned reporting, documentation and quality standards.\n, • External Engagement and Governance: Represent the laboratory in governance forums; contribute to external regulatory interactions; lead capability-building in diagnostic pathology and companion diagnostics across matrix teams.\n Essential Skills/Experience:\n \n, • Medical degree recognised by the General Medical Council (GMC).\n, • Current Licence to Practice in the United Kingdom.\n, • Significant experience practising at consultant pathologist level, or equivalent senior medical pathology role, within a diagnostic or regulated laboratory environment.\n, • Experience providing medical and technical oversight for testing within an accredited or regulated laboratory environment.\n, • Strong working knowledge of CAP/CLIA, ISO 15189, GCP, IVDR, HTA and applicable standards governing laboratory quality systems, patient testing, and report issuance.\n, • Experience reviewing, authorising, or providing medical oversight of laboratory reports, ensuring outputs are scientifically valid, medically appropriate, and compliant with regulatory and quality requirements.\n, • Ability to provide clear clinical and scientific interpretation of pathology and biomarker data, integrating findings with other data streams where relevant.\n, • Strong leadership, communication, and stakeholder management skills, with the ability to work effectively across matrix teams and provide oversight to multidisciplinary laboratory activities.\n Desirable Skills/Experience:\n \n, • GMC Specialist Registration in an appropriate pathology specialty.\n, • FRCPath in Histopathology or another relevant pathology discipline, or equivalent specialist qualification.\n, • PhD, MD(Res), or equivalent higher research qualification in pathology, oncology, translational medicine, biomarker science, or a related discipline.\n, • Experience in companion diagnostic and predictive biomarker development within pharmaceutical, biotechnology, or accredited diagnostic laboratory settings, working in line with ISO 13485 and ISO 14971.\n, • Experience serving in a role aligned to CAP Technical Supervisor, General Supervisor, or Laboratory Director responsibilities for high-complexity testing.\n, • Familiarity with digital pathology, image analysis, and computational pathology approaches in a regulated environment.\n, • Experience with diagnostic methods, such as PCR, NGS, spatial omics, proteomics, mass spectrometry and other platforms relevant to precision medicine.\n, • Experience leading or supporting clinical trial assay governance, including oversight of testing strategies, report processes, and protocol-aligned patient testing.\n, • Experience overseeing or contributing to prospective patient testing in support of clinical trials, including understanding of protocol-driven testing, result reporting, and documentation requirements.\n Why AstraZeneca:\n Here, your expertise in diagnostic pathology fuels a bold mission: detecting disease earlier, matching patients to targeted treatments and tackling some of the toughest cancers through science and technology. With a deep, well-funded pipeline and teams empowered to make smart, fast decisions, we bring clinicians, data scientists and engineers together to turn breakthrough ideas into validated tests that shape studies and patient outcomes. You will find the ambition to push boundaries balanced with a culture that values collaboration and kindness—so you can lead, learn and see the real-world impact of your work every day. \n Lead the evolution of diagnostics that guide life-changing medicines—take the next step in your career and shape how patients are identified and treated. Date Posted\n 14-Aug-2026 Closing Date\n 27-Aug-2026 \n Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form. \n #J-18808-Ljbffr

Job Title: Director of Pathology Location: Cambridge, UKHybrid working: Minimum 3 days per week in the officeIntroduction to role: Are you ready to bring decisive medical leadership in pathology to accelerate personalised diagnostics that guide clinical trials and patient care? This is a chance to shape how novel biomarkers become trusted tests that identify the right patients for the right therapies, faster. You will join our internal accredited laboratory delivering in-house diagnostic testing for early-phase clinical studies and pioneering approaches in patient stratification. Your oversight will ensure assays are robust, validated and clinically meaningful, directly influencing how our medicines are developed and how patients are selected for studies. Working at the intersection of pathology, quality, and translational science, you will help advance companion and complementary diagnostics— including computational pathology and image analysis—across a biomarker-driven portfolio. At Director level, you will look beyond daily operations to set direction, influence governance, and represent the laboratory in internal and external forums. Will you help us lift diagnostic standards, bring new technologies into practice, and translate cutting-edge science into results that clinicians and patients can trust?Accountabilities: - Medical and Technical Oversight: Provide pathology oversight of assay performance, result review and reporting practices in an accredited environment supporting clinical and biomarker development. - CAP/CLIA and GxP Compliance: Act in a role aligned to CAP/CLIA expectations; ensure testing and reporting practices meet regulatory and professional standards, including ISO 15189, GCP, IVDR and HTA requirements. - Result Authorisation and Interpretation: Review, interpret and approve laboratory results and reports, ensuring outputs are scientifically valid, clinically appropriate and compliant with defined quality requirements; contribute to clinical and scientific interpretation of pathology and biomarker data. - Method Evaluation and Approval: As technical lead, evaluate and approve novel test methods; ensure fitness for purpose and appropriate validation or verification before clinical use. - Operational Partnership: Work closely with the Laboratory Director, QA/QC and operational leadership to evolve methods, procedures, instrumentation, staffing models and workflow design. - Strategy and Companion Diagnostics: Provide scientific and medical input into assay and biomarker strategy, including companion diagnostic development and clinical implementation planning; align with broader clinical development objectives. - Innovation and Digital Pathology: Drive continuous improvement and the introduction of emerging technologies, including digital pathology, image analysis and data-enabled diagnostic workflows. - Clinical Trial Support: Provide medical and technical oversight for prospective patient testing in clinical studies, ensuring protocol-aligned reporting, documentation and quality standards. - External Engagement and Governance: Represent the laboratory in governance forums; contribute to external regulatory interactions; lead capability-building in diagnostic pathology and companion diagnostics across matrix teams. Essential Skills/Experience: - Medical degree recognised by the General Medical Council (GMC). - Current Licence to Practice in the United Kingdom. - Significant experience practising at consultant pathologist level, or equivalent senior medical pathology role, within a diagnostic or regulated laboratory environment. - Experience providing medical and technical oversight for testing within an accredited or regulated laboratory environment. - Strong working knowledge of CAP/CLIA, ISO 15189, GCP, IVDR, HTA and applicable standards governing laboratory quality systems, patient testing, and report issuance. - Experience reviewing, authorising, or providing medical oversight of laboratory reports, ensuring outputs are scientifically valid, medically appropriate, and compliant with regulatory and quality requirements. - Ability to provide clear clinical and scientific interpretation of pathology and biomarker data, integrating findings with other data streams where relevant. - Strong leadership, communication, and stakeholder management skills, with the ability to work effectively across matrix teams and provide oversight to multidisciplinary laboratory activities. Desirable Skills/Experience: - GMC Specialist Registration in an appropriate pathology specialty. - FRCPath in Histopathology or another relevant pathology discipline, or equivalent specialist qualification. - PhD, MD(Res), or equivalent higher research qualification in pathology, oncology, translational medicine, biomarker science, or a related discipline. - Experience in companion diagnostic and predictive biomarker development within pharmaceutical, biotechnology, or accredited diagnostic laboratory settings, working in line with ISO 13485 and ISO 14971. - Experience serving in a role aligned to CAP Technical Supervisor, General Supervisor, or Laboratory Director responsibilities for high-complexity testing. - Familiarity with digital pathology, image analysis, and computational pathology approaches in a regulated environment. - Experience with diagnostic methods, such as PCR, NGS, spatial omics, proteomics, mass spectrometry and other platforms relevant to precision medicine. - Experience leading or supporting clinical trial assay governance, including oversight of testing strategies, report processes, and protocol-aligned patient testing. - Experience overseeing or contributing to prospective patient testing in support of clinical trials, including understanding of protocol-driven testing, result reporting, and documentation requirements. When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. Why AstraZeneca: Here, your expertise in diagnostic pathology fuels a bold mission: detecting disease earlier, matching patients to targeted treatments and tackling some of the toughest cancers through science and technology. With a deep, well-funded pipeline and teams empowered to make smart, fast decisions, we bring clinicians, data scientists and engineers together to turn breakthrough ideas into validated tests that shape studies and patient outcomes. You will find the ambition to push boundaries balanced with a culture that values collaboration and kindness—so you can lead, learn and see the real-world impact of your work every day. Lead the evolution of diagnostics that guide life-changing medicines—take the next step in your career and shape how patients are identified and treated.Date Posted14-Aug-2026Closing Date27-Aug-2026Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.SummaryLocation: UK - CambridgeType: Full time

At Samsung Cambridge Solution Centre (SCSC) we develop world-leading Bluetooth and Wi‑Fi connectivity solutions which are designed into a wide range of both mobile and non‑mobile applications worldwide. The Architecture & Digital Design (ADD) team are involved throughout the product lifecycle and cover aspects such as Bluetooth/Wi‑Fi standards, product specification, systems algorithm design, hardware IP architecture, digital design & verification, radio optimisation, and customer support. We are looking to hire an experienced hardware IP architect into the team who can us help to identify and implement complex performance, power, and area (PPA) enhancements across our wireless IP solutions. • Work with leaders, architects, and engineers across the business to scope and implement complex new features, • Analyse existing features and identify potential PPA enhancements based on evolving customer requirements, • Follow market trends and recognise opportunities for future innovative solutions Required • Detailed knowledge of modern SoC architectures including components such as processors, bus interconnects, DMA engines, and internal/external interfaces (AXI, AHB, PCIe, USB, UART etc.), • Excellent ability to author and maintain technical documentation, and proven ability to write reference material for a wide variety of stakeholders (e.g. designers, users, product owners etc.), • Strong IP modelling/prototyping capabilities which allow key architectural changes (e.g. processor, memory sizing, bus interconnects, clock frequencies etc.) to be adopted with maximum confidence, • In depth knowledge of wireless system partitioning (e.g. software vs. hardware, firmware vs. host etc.), • Experience of wireless protocol operation, a good understanding of the key customer operating modes, and their impact on PPA optimisation, • Experience with RISC CPU microarchitectures (including Arm A/R/M cores) and associated peripherals (e.g. interrupt controllers, cache controllers etc.), • Experience in SystemVerilog hardware design and/or embedded programming in C, • Experience of hardware prototyping techniques, • Experience with wireless security mechanisms and their impact on hardware architectures, • Experience of digital signal processing (DSP), specifically the trade-offs between hardware/software, and the impact on RF circuit design Joining our team, you'll receive a great benefits package. • Annual bonus, • Continued training and development, • Private medical insurance, • Travel insurance, • Life insurance, • Flexible benefits system, • 25 days holiday with the option to buy or sell days, • Great discounts on Samsung products, • Free on‑site gym and canteen We know that the diversity of our team is integral to our continued success. We encourage people to apply from all backgrounds. Please let us know if you need any reasonable adjustments to take part in this recruitment process and we'll do our best to arrange these if needed. #J-18808-Ljbffr

ABOUT YOUThe position requires a highly organised and detail-oriented professional who thrives in a fast-paced, client-facing environment. You will be confident managing multiple priorities, building strong stakeholder relationships, and ensuring a consistently high level of service delivery.You will ideally bring a scientific background alongside strong communication and project coordination skills, with the ability to translate technical information into clear, client-friendly language.You will also have knowledge of cGMP regulations and pharmacopoeia to ensure that operations are carried out in line with required standards where applicable.Required skills and experience:Educated to a Higher Education level in a relevant discipline (e.g. Chemistry or related), with laboratory exposureProven experience working within a laboratory or scientific environmentUnderstanding of project management principles and ability to coordinate multiple workstreamsStrong communication and presentation skills, with confidence engaging stakeholders at all levelsAwareness of cGMP regulations and pharmacopoeia requirementsExperience within analytical chemistry environments (e.g. HPLC / LCMS) would be highly advantageousExperience managing or supporting inhaled or biologics projects is desirableExcellent organisational, time management and IT skills (Microsoft Office)Strong attention to detail with a proactive, solutions-focused mindsetAbility to deliver exceptional customer service and build lasting client relationshipsPositive, adaptable approach with a genuine desire to learn and developABOUT THE OPPORTUNITYTo perform the role and responsibilities of a Project Manager within the laboratory environment, acting as the primary liaison for clients throughout the full project lifecycle.You will take ownership of project delivery end-to-end, ensuring projects are delivered on time, to quality, and to client expectations. This includes defining project scope, supporting quotation development, and working closely with internal teams to meet delivery commitments.You will play a key role in bridging laboratory teams and clients, translating complex scientific activity into clear, structured updates while supporting commercial objectives.Key activities:Act as the primary point of contact for all assigned client projects, managing project organisation and administration end-to-endMonitor project progress against agreed KPIs and milestones (internal and external), proactively managing risks and resolving issuesDefine and agree project deliverables with clients, ensuring clarity from initiation through to completionSupport project setup, including preparation of documentation, protocol writing/review, and assessment of equipment and consumablesDevelop a strong understanding of each client project, including the purpose of the drug and how analysis fits within the wider development programmeProvide clear, consistent communication and progress updates to stakeholders, translating technical information into client-friendly languageOrganise and lead project meetings, including preparation of slides, minutes, action logs, risk logs and issue trackingCollaborate with cross-functional teams to resolve technical or contractual queries throughout the project lifecycleMonitor in-process activities and keep senior management informed, including key metrics such as:Testing and report turnaround timesOn-time deliveryWHAT WE OFFERJoin Intertek and become part of our global network of inspiring and entrepreneurial colleagues. We are a global family that values diversity and we thrive working together with precision, pace, and passion. We are working to make the world Ever Better, ensuring the quality, safety and sustainability of products and services used by millions of people around the world.Competitive salary/benefits Development and career opportunities around the Globe Working in a highly motivated team and dynamic working environmentWe are an Equal Opportunity Employer and are committed to creating an inclusive workplace. We do not discriminate against applicants, and all qualified individuals will receive consideration for employment regardless of age, disability, gender reassignment, marriage or civil partnership, pregnancy or maternity, race, colour, nationality, ethnic or national origin, religion or belief, sex, or sexual orientation. We are committed to fair and equitable pay and are proud to be a Real Living Wage employer, ensuring our colleagues are compensated in line with independently assessed living standards. We are also committed to providing reasonable adjustments throughout the recruitment process and employment to support candidates and employees with disabilities or special needs. Intertek operates a preferred supplier arrangement, and we do not accept unsolicited approaches from agencies. Full timePosting Date: 2026-07-21

This role involves ensuring compliance with the protocol, monitoring sites, and supporting data integrity. The Origin Group Ltd in Cambridge is seeking a Study Monitor / Clinical Research Associate to oversee clinical studies.

SoCode Limited is seeking a junior to mid-level embedded software engineer for a hybrid or on-site role in Cambridgeshire. You will work in C/C++ on protocol stacks and embedded systems, supporting wireless technologies such as 5G and LTE.

Protocol National ltd trading as Protocol are acting as an employment business for this position. If you are successful, Protocol is required to see evidence of your Right to Work in the UK; in addition to you applying for an enhanced DBS Certificate should you not already hold a suitable certificat

The Clinical Manager will own the end-to-end delivery of Sequential's clinical study portfolio from feasibility and protocol development through ethics approval, recruitment, study conduct, database lock and close-out. The Clinical Manager will also build reusable systems for future projects of a si

Protocol is seeking a Learning Support Mentor / Learning Support Assistant to join our Further Education team in Cambridge. You will provide dedicated 1:1 and small-group support to learners with SEND, learning difficulties, and other needs, helping them reach their potential. You'll work alongside

Protocol National ltd trading as Protocol are acting as an employment business for this position. Protocol is specifically seeking local Lecturers/Assessors to add to the database to work in FE Colleges in Cambridge and the surrounding areas. Protocol is proud to be Disability Confident Committed.

Job Description Summary#LI-HybridLocation: CambridgeThe Clinical Sciences Associate Director may provide clinical leadership and strategic input for all clinical deliverables across assigned indication/program or studies within BR. May act as Focus/Disease/Platform Area Lead. May function as a Core Project Team member for assigned projects to drive the Research-Development- Commercial (R-D-C) continuum. May co-lead project clinical sub-team and reports study/project progress and issues with their resolution plan to project teams and stakeholders. Directs early stages of study design and operational plansJob DescriptionKey Responsibilities: Study Leader and/or Clinical Scientist for predominantly high complexity, global studies and may provide additional Clinical Sciences support to high priority, high complexity, global studies.Independently lead the clinical protocol development process in collaboration with the Medical Lead and other line functions; responsible author for clinical protocols, amendments, etc.; contribute to the medical/scientific input given for the development of study-related documents and processes which reside in other line functions; contribute to the development of clinical sections of study-level regulatory documents.Lead development of strategic and scientific input into study concept, feasibility, and ability to execute; develop and implement study-level operational execution plan in partnership with key cross functional partners, if applicable.Collaborate with key cross functional partners to identify and select strategic and high performing sites to ensure recruitment commitments are met.Lead a global cross functional Clinical Trial Team (CTT) to ensure all trial deliverables are met; set stretch goals, promote realistic planning and timelines, and presents actionable alternatives to accelerate timelines.Partner with line functions to gain input and alignment and manages internal and external stakeholder expectations.Lead the ongoing medical/scientific review of clinical trial data across assigned studies in collaboration with the medical expert and key line functions, and partners on data analysis and data interpretation, including safety trend analysis, signal detection, development of first interpretable results, reporting clinical study results in Clinical Study Report (CSR), and internal/external publications.Prepare and lead dose escalation meetings with investigators. Coordinate the real time availability of quality clinical trial data, to provide consolidated information for dose escalation meetings and Phase II data reviews with relevant stakeholders.Proactively lead risk mitigation discussions, risk management and implementation at the trial level.Responsible and accountable for forecasting and managing overall study budget(s) in collaboration with key partners.Collaborate with key partners to set vendor strategy and timelines for assigned studies.Responsible for implementation of best practices and standards for trial management, including sharing lessons learned. Represent group on initiatives; may serve as Subject Matter ExpertContribute to talent and career development of staff. In collaboration with the relevant manager, contribute to hiring/interview/onboarding and mentoring process for new hires.Line management of assigned associates. Accountable for talent attraction and retention; supporting career growth and development.May deputize for his/her manager upon request.Essential Requirements: Bachelors in life science/healthcare required; Advanced degree or equivalent education/degree in life sciences/ healthcare preferred (PhD/MD/PharmD/ Masters).8+ years’ experience in clinical trials/development.Demonstrates high learning agility in multiple therapeutic areas.Demonstrated knowledge and ability to confidently drive complex collaborations through unpredictable circumstances and higher paced changes.Demonstrates leadership and influence by creating a positive work environment by inspiring and encouraging mutual respect, instills innovation and accountability on a functional and trial level.Strong interpersonal skills with a proven track record of successfully interacting with and influencing with a wide range of people, building strong positive relationships.Demonstrates strong organizational awareness and stakeholder management skills.Demonstrate strong tolerance for ambiguity, willingness to adapt, and willingness to speak-up and challenge.The salary for this position is expected to range between $152,600 and $283,400 per year.The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.To learn more about the culture, rewards and benefits we offer our people click here.EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.Salary Range$152,600.00 - $283,400.00Skills DesiredBudget Management, Clinical Research, Clinical Trials, Coaching, Data Analysis, Learning Design, Risk Management, Risk MonitoringSummaryLocation: Cambridge (USA)Type: Full time

Principal/Senior Software Engineer | Embedded Wireless Systems Cambridge (Hybrid / On-site) | £80,000 base + bonus Are you ready to take your embedded software career to the next level? Join a dynamic engineering team working on advanced wireless systems and communication protocols used in real-world networks. This is a hands-on role where your work directly shapes products from concept to deployment. Why You’ll Love This Role: Own the technology: Influence architecture and design across complex embedded wireless systems Stay hands-on: Work in C/C++ on protocol stacks and hardware integration Grow as a leader: Mentor and support engineers while driving best practices Make an impact: Solve challenging, real-world problems in wireless communications Flexible, collaborative environment: Small, highly skilled team focused on innovationWhat We’re Looking For: 5+ years’ experience in embedded software development Strong C/C++ skills in embedded environments Knowledge of cellular or wireless communication protocols (5G, LTE, or legacy) Experience with full product lifecycle: design, testing, deployment, support Strong problem-solving, collaboration, and communication skills Desire to mentor others and grow in a technical leadership roleBonus Skills: Exposure to signal processing or hardware interfaces Familiarity with CI/CD pipelines (TeamCity, Jenkins, etc.) Experience writing technical documentationReady to Take the Next Step? This is a rare opportunity to join a small, ambitious team where your ideas and expertise truly shape the products you work on. Apply today with your CV or send a message for a confidential discussion. Don’t wait - your next career move starts here

Junior / Mid Software Engineer | Embedded Wireless Systems | Cambridgeshire (Hybrid / On-site)Cambridgeshire (Hybrid / On-site) Paying up to £55,000 Are you ready to grow your embedded software career in wireless communications? Join a small, highly skilled engineering team working on advanced wireless systems and communication protocols used in real-world networks. This is a hands-on role where your work directly contributes to products from development to deployment. Why You’ll Love This Role: Learn and build: Work in C/C++ on protocol stacks and embedded systems Grow your skills: Gain experience with wireless technologies like 5G, LTE, or other cellular standards Hands-on impact: Contribute to real-world wireless systems and help solve challenging technical problems Collaborative environment: Work closely with experienced engineers in a supportive, flexible teamWhat We’re Looking For: 2–4 years’ experience in software development (C/C++) Exposure to embedded or systems-level programming Some knowledge of cellular or wireless communication protocols Comfortable working with existing codebases and software platforms Strong problem-solving, collaboration, and communication skills Right to work in the UK Ready to Take the Next Step? This is a rare opportunity to develop your career in wireless systems alongside an experienced engineering team. Your contributions will be hands-on, meaningful, and visible across real-world projects. Apply today with your CV or send a message for a confidential discussion

SEN Teaching Assistant Opportunities – Harrow & Brent Location: Harrow & Brent School Type: Primary Mainstream Schools Contract: Full-Time & Part-Time | Flexible Supply & Long-Term Roles Start Date: Immediate / September Make a Difference Every Day! Protocol Education is recruiting SEN Teac

Protocol Education are recruiting for a Level 3 Qualified Early Years Practitioner / Room Leader to join a welcoming nursery in Camden from September 2026.

The Protocol Group is seeking an Interim Payroll Manager to cover a busy college payroll function in Hull.

For details of our Privacy Policy, please visit the Protocol Education website. Protocol Education is working with a friendly and supportive primary school in. Why Work Through Protocol Education?.

Protocol is seeking passionate Business Lecturers to join a pool of talent for FE teaching opportunities across South Yorkshire for the new academic year.

Please see the FAQs on the Protocol Education website for further details. Protocol Education is committed to safeguarding and promoting the welfare of children. For details of our privacy policy, please see visit the Protocol Education website.

An educational support agency is seeking a Psychology Graduate for a Teaching Assistant role in Shrewsbury, supporting young individuals with special educational needs and mental health challenges.This full-time position offers £90–£95 per day, starting September 2025.Ideal candidates are empath

Protocol is building a talent pool of English Lecturers for anticipated vacancies across Further Education colleges in South Yorkshire for the upcoming academic year.

Protocol Education is actively recruiting flexible Early Years Practitioners to support nurseries across Camden on a supply basis.

The Protocol Group is an equal opportunities employer and is committed to providing an inclusive and professional service for all. If you are successful, Protocol is required to see evidence of your Right to Work in the UK; in addition to you applying for an enhanced DBS Certificate should you not a

Invites to Protocol Education coffee mornings and events hosted for candidates. Please see the FAQs on the Protocol Education website for further details. Protocol Education is committed to safeguarding and promoting the welfare of children.

A dedicated education service provider is seeking a SEND Specialist Teacher in the United Kingdom.You will be working with pupils aged 3–19 who have complex learning needs, delivering a customized curriculum to foster their independence and confidence.Key responsibilities include lesson planning,

The Protocol Group is an equal opportunities employer and is committed to providing an inclusive and professional service for all.

Protocol Education Ltd is seeking a flexible Nursery Practitioner in Islington to support daily care and early years learning for children aged 0-5.

Programme Tutor Assessor (Data & AI).Hull / Grimsby / Hybrid / Online.Help Shape the Future of Data & AI Talent.Are you passionate about Data, Artificial Intelligence, and developing the workforce of tomorrow?.We are looking for an experienced and motivated.Programme Tutor Assessor (Data & AI).This

Protocol Education is working with a friendly primary school in Downend seeking a dedicated Behaviour Mentor to support pupils with behaviour, emotional wellbeing, and engagement in learning.

Whether you're an experienced teacher, an Early Career Teacher (ECT), or returning to the classroom after a break, Protocol Education has opportunities across Huddersfield that fit around your life. Apply today with your CV or contact our local Protocol Education team for an informal chat about the

Protocol Education is seeking Early Career Teachers (ECT) who have finished their PGCE to start this September.

Protocol Education is seeking a Level 3 Nursery Practitioner to join a welcoming nursery in England.

For details of our privacy policy, please see visit the Protocol Education website. Please see the FAQs on the Protocol Education website for further details. Protocol Education is committed to safeguarding and promoting the welfare of children.

Protocol Education is seeking an English graduate to join a specialist SEND school in Gateshead.

Protocol Education is recruiting sports graduates and professionals to support children across Wiltshire.

Protocol Education is seeking a Nursery Practitioner to join our caring team in England.

Why work with Protocol Education?. Please see the FAQs on the Protocol Education website for further details. Protocol Education is committed to safeguarding and promoting the welfare of children.

Please see the FAQs on the Protocol Education website for further details. Protocol Education is committed to safeguarding and promoting the welfare of children. For details of our privacy policy, please see visit the Protocol Education website.

Business Lecturers - Further Education.Temporary, Contract, Permanent Opportunities Available.Competitive, dependent on experience and qualifications.Further Education? We are building a talent pool of outstanding Business professionals for a range of exciting teaching opportunities across colleges

Protocol Education is recruiting a full-time Autism Specialist Learning Support Assistant to join a specialist provision in Longbenton.

Protocol in Hull/Grimsby offers a full-time Programme Tutor Assessor (Data & AI) role across hybrid and online delivery.