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Business Manager – Brand New State-of-the-Art Hospital Up to £55,000 DOE + Competitive Company Benefits Oxford Want to be a key part in the opening and success of a BRAND NEW and state of the art hospital? Compass Associates are proud to have exclusively partnered with Welbeck Health Partners for the opening of their brand-new hospital, boasting 12 specialties equipped with the latest technology and world-renowned consultants dedicated to delivering the best patient experience. Capitalising on the success of their London flagship hospital, their new site will offer a wide range of medical diagnostic and same-day minimally invasive services, including heart health, lung health, digestive health, ENT, endoscopy, and neurology. This is a very exciting opportunity for an individual who wants to help to shape a growing, but established healthcare organisation. Welbeck Health Partners was founded by leading healthcare specialists from the UK and USA who shared a clear vision: to deliver better care and redefine what a healthcare organisation can be. Welbeck’s unique partnership model empowers clinicians to share in the success of the group while fostering a collaborative environment. It provides a framework for consistent patient pathways, quality assurance across partners, and smooth cross-referrals between specialties. Joining Welbeck means becoming part of a growing network of high-quality clinics and world-leading healthcare professionals. Welbeck are committed to creating a supportive, values-driven environment where their people can thrive. The company invests in its people, providing ongoing professional development, clear career progression, and the resources needed to excel. If you’re looking to be part of a purpose-led organisation that is shaping the future of healthcare while fostering a culture of respect, teamwork, and shared success, we’d love to hear from you. What is in it for you? • Paid for park and ride, • Great work-life balance, • Professional registration paid for annually, • Personal Development Plan, • 27 Days Annual Leave + Bank Holidays, • Private Medical Insurance, • Eye Care, • Annual Flu Vaccines, • Private Pension, • Season Ticket Loan / Cycle to Work Scheme, • Employee Assistance Programme, • AND a range of policies supporting health and wellbeing We are seeking an experienced and dynamic Senior Manager with exceptional interpersonal and leadership skills. This is a unique opportunity to play a key role in establishing and growing one of the most exciting developments within the Welbeck Health Partners network. You will work alongside leading consultants across multiple specialties to deliver outstanding patient care and operational excellence. As the centre develops and expands, this role offers significant scope for professional growth and the opportunity to contribute to shaping the future of premium healthcare delivery in the Oxfordshire region. The post holder will be expected to support their team, department and centre to achieve the Welbeck Values in their day-to-day work. They will provide a responsive and efficient administrative service to meet the needs of the Business. You will be an effective decision maker, who is able to prioritise their own workload whilst responding to interruptions. The post holder will be able to deal with unpredictable work patterns and proactively deal with issues without reference to others. Responsibilities: • Overall responsibility for all business functions, including budget control, operational management of patient pathways, and billing/accounting., • Line-manage the Front of House and Administration teams, including lead administrators, receptionists, billing staff, and clinical/consultant administrative teams., • Promote a patient-centred approach, upholding exceptional customer service principles throughout the patient journey., • Ensure all staff are appropriately inducted, trained, and supported with the necessary resources to perform effectively., • Identify and address training and development needs for staff, ensuring performance appraisals and development plans are completed in line with policy., • Recruit suitable candidates for Front of House, Administration, and clinical support roles as required., • Support the Centre Director, Clinical Service Director and Operations Director in identifying new business opportunities, service redesign initiatives, and operational improvements focused on patient care., • Use service improvement techniques, audit processes, and data analysis to monitor and enhance service delivery., • Engage proactively with service users, clinical teams, and key stakeholders to ensure feedback informs service planning and continuous improvement., • Assist in implementing and maintaining clinical governance, complaints, and risk management processes, monitoring compliance with regulatory standards and best practice., • Support clinical staff in root cause analyses of complaints, incidents, and operational issues, ensuring timely resolution and learning., • Collect, interpret, and report on data relating to service performance, patient satisfaction, and operational efficiency, recommending corrective actions as necessary., • Ensure appropriate administrative and operational coverage in line with service needs, including contingency planning., • Oversee debt collection reporting and management, working with internal teams and external agencies to optimise financial performance., • Adopt a data-driven approach to decision-making to improve services objectively and effectively., • Develop and maintain effective communication channels across teams to foster collaboration, engagement, and a high-performing work culture, • Ensure compliance with HR, health & safety, and regulatory requirements across all business functions., • Champion a culture of continuous improvement, innovation, and operational excellence throughout the service. Recommendations We’re currently recruiting for a variety of management, clinical, and non-clinical roles across Oxford and Cambridge. If this role isn’t for you but you are interested in exploring other opportunities, feel free to share your details. If you know someone who may be interested in this or other roles in a new private hospital, we offer a £200 voucher referral reward for every successful recommendation.

Overview Pictura Bio is a well-funded University of Oxford spin-out developing a novel diagnostic platform for rapid pathogen detection. Our technology combines fluorescence microscopy with automated image analysis and machine learning to identify pathogens in seconds. The platform is being translated into clinical diagnostic products, initially focused on respiratory infections, with broader applications across infectious disease. Role Purpose The Clinical Validation Lead will be responsible for designing, executing, and overseeing clinical and analytical validation of Pictura Bio’s diagnostic assays. You will lead validation strategy from late-stage development through clinical evaluation, ensuring studies are scientifically robust, regulator-ready, and aligned with the intended clinical use. This role is ideal for someone with hands-on experience validating diagnostic assays in regulated environments, particularly US LDTs, but experience with FDA-cleared/approved, UK, or EU IVD pathways is also highly relevant. You will work closely with assay development, data science, regulatory, and external clinical partners. Major Accountabilities · Lead the design and execution of analytical and clinical validation studies for diagnostic assays · Define validation plans covering precision, accuracy, sensitivity/specificity, LoD, reproducibility, interference, and cross-reactivity · Ensure validation studies are aligned with intended use, clinical claims, and regulatory expectations · Oversee clinical sample selection, handling, and testing in collaboration with partner laboratories and CROs · Support validation of Laboratory Developed Tests (LDTs), particularly within the US regulatory framework · Contribute to validation supporting FDA (e.g. De Novo / 510(k)), UKCA, or CE-IVD pathways where applicable · Review and approve protocols, reports, and data summaries for internal and external use · Work with data science teams to ensure clinical performance metrics and analyses are appropriate and traceable · Interface with regulatory and quality teams to support technical files, submissions, and audits · Manage external stakeholders (clinical sites, reference labs, CROs) involved in validation activities · Clearly communicate validation strategy, results, and risks to senior leadership Ideal Background Education · PhD, MD, PharmD, or MSc in a relevant discipline (e.g. Clinical Sciences, Biomedical Sciences, Molecular Biology, Immunology, Microbiology) Experience · Demonstrated experience clinically validating diagnostic assays · Experience with assays such as immunofluorescence, molecular diagnostics, NGS / optical sequencing (e.g. Illumina), or imaging-based diagnostics · Experience developing or validating US Laboratory Developed Tests (LDTs) is highly desirable · Experience supporting FDA-cleared/approved assays (De Novo, 510(k), PMA) or UK/EU IVD pathways is advantageous · Experience working with clinical samples (e.g. respiratory samples, blood, urine, swabs) · Experience collaborating with hospital labs, reference labs, or CROs Skills · Deep understanding of diagnostic validation principles and study design · Strong knowledge of clinical performance metrics and statistical interpretation · Familiarity with regulatory and quality frameworks (e.g. CLIA, CAP, ISO 13485, ISO 15189) · Ability to translate clinical requirements into practical validation studies · Strong documentation, reporting, and review skills · Excellent communication skills, including interaction with clinicians, regulators, and executives Desirable Personal Attributes · Highly organised and detail-oriented, with a strong quality mindset · Comfortable taking ownership of complex, multi-stakeholder validation programmes · Scientifically rigorous but pragmatic in balancing timelines and regulatory expectations · Confident communicator who can explain validation decisions clearly · Comfortable working in a fast-moving, scaling diagnostics company

Job Title: Occupational Health Nurse Manager Location: Oxford, OX4 Salary: £52,000 - £57,000 per annum Contract Type: Permanent Hours: Full Time, 37.5 hours per week. Monday- Friday (7.5 hours per day) About Us Optima Health are the UK market leader of Occupational Health and Wellbeing services. Our heritage can be traced back to 1947 where we were pioneers in the provision of Occupational Health and have led the way ever since, bringing new and innovative solutions to employers across the UK. We can offer unrivalled clinical expertise and industry leading tailored solutions to our clients. We work with over two thousand businesses, in various industries, and our aim is to improve the health and wellbeing of the UK workforce by supporting healthy high performance in our client organisations, helping them to achieve their full potential through their people. Optima Health not only provide an excellent package, but we also offer a structured induction and training programme in your first few weeks. We offer tailored career development and opportunities for further training and qualifications, to support you in your career journey. We are committed to making this a really great place to work, so together, we live by our values; We are one team, we do the right thing, we are shaping tomorrow, and we are never too big to care. Role Summary The Occupational Health Manager will be responsible for the overall management and performance of occupational health services for a prestigious client within the automotive manufacturing sector. This is a predominantly management-focused role, providing leadership, clinical supervision, and line management to an on-site, multi-disciplinary clinical team. The role requires proven experience in managing complex health surveillance programmes, overseeing service delivery, and ensuring consistently high clinical standards. While the primary focus is on leadership and performance management, the OH Manager will also provide ad hoc case management and expert clinical input for complex or high-risk cases as required. Working closely with senior client stakeholders, the OH Manager will build strong partnerships to deliver agreed occupational health and wellbeing objectives. The role includes monitoring performance against benchmarked targets, driving continuous improvement, and ensuring services are compliant with evidence-based practice, legislative requirements, and clinical governance standards. There will also be an expectation to visit other sites (Wiltshire, Hampshire and West Midlands) on a quarterly and ad hoc basis to ensure OH services are delivered to a high standard. Expenses are reimbursed. Who Are We Looking For? • Experience of managing Occupational Health contracts as a Clinician, • Experience of managing health surveillance programmes, • Qualification in Occupational Health, • Clinical qualification as Nurse with registration with relevant professional body (NMC or HCPC)., • Experienced in Occupational Health clinical delivery as Occupational Health Advisor or similar, • Experience of managing a multi-disciplinary team of clinical and no clinical employees., • Experience of using data as a tool to take the service forward., • Effective communication and negotiation skills. What Can We Offer You? • Competitive salary, • 25 days annual leave, plus bank holidays, • Buy and sell holiday scheme, • Pension scheme, • Health Cash Plan, • Career progression opportunities, • Employee Assistance Programme, • Cycle to work scheme, • Eye care test vouchers, • Flu vaccination scheme, • Employee discount scheme, • Life assurance, • Professional registrations fees paid, • Clinical Training Academy, • Save as you earn scheme, • Yulife Optima Health is committed to creating a diverse and inclusive environment and is proud to be an equal opportunity employer. All applicants meeting the minimum criteria for the role will receive consideration for employment without regard to age, gender or gender expression, disability, race or ethnicity, religion or belief or sexual orientation.

Physiomics Physiomics plc (AIM: PYC) is an Oxford-based contract research organisation and consultancy specialising in the application of mathematical and data science solutions to support the development of therapeutic drugs and personalised medicine dosing software. Physiomics has a current turnover of circa £1m p.a. It has a high-profile brand and an established customer base of clients in the UK, Europe and North America. Physiomics takes a collaborative approach to provide clients with bespoke solutions encompassing data, analytics and insight. Physiomics is structured in two service-lines; Model Informed Drug Development (MIDD) and Biometrics. The Company’s MIDD service-line provides a full range of pharmacokinetic/ pharmacodynamic contract services to companies ranging from biotechs to some of the largest pharmaceutical companies in the world, across multiple therapeutic areas. The Company uses a range of commercially available software solutions but also maintains its own proprietary Virtual Tumour™ model which simulates the effects of anti-cancer agents on pre-clinical and human tumours, helping clients to improve the success rate of drug discovery and development projects while reducing time and cost. The MIDD service-line has completed over 140 commercial projects, involving over 125 targets and drugs, and has worked with clients such as Merck KGaA, Numab Therapeutics, Cancer Research UK and Bicycle Therapeutics, to name but a few. The Company recently expanded its contract services into the field of Biometrics, which is run as a separate service-line and provides biostatistics, statistical programming and data management solutions. Even though only recently launched, this service-line is already delivering on several client contracts and has a rapidly growing pipeline of opportunities being progressed. Separately from its contract services business, Physiomics has won several Innovate UK and NIHR grants which it has used to develop a software tool to personalise the dose of chemotherapy. It has an ongoing collaboration with US company, DoseMe, and has incorporated this tool into their existing commercial platform (DoseMeRx). The dosing software tool is currently available for research use only, but as the tool is further developed, the plan is to implement paid for functionality. The CEO Role Physiomics is seeking a new leader to drive an ambitious program of expansion and strategic change within an LSE AIM-listed business. The role requires excellent influencing skills, keen commercial acumen and the ability to communicate effectively with both scientific/ clinical and commercial stakeholders. Even though prior experience is not necessary, the role will be responsible for managing all corporate activities pertaining to being a public company, work with the board of directors, Company Secretary, NOMAD and Broker to ensure compliance to AIM rules and effective governance of the business. Physiomics’ revenues are derived mostly from its core contract services business, and this will remain the first priority of the incoming CEO who will be able to support the acquisition and retention of clients, participate in key meetings and presentations, lead the internal team and have the experience and gravitas to act as a senior advisor to key client contacts. The Company currently operates virtually, although the CEO will need to be available for regular face to face team meetings in the Oxford / London area. The role will require occasional travel (in the UK and abroad) to clients, networking activities, and meetings with stakeholders. The company currently has 12 permanent employees (including Board Directors) and utilises contractors to provide additional capacity and expertise when required. The Company operates a fee for service revenue model but has developed a personalised dosing tool that could form the basis of a software-as-a-service offering. Physiomics believes this role represents a real opportunity for the right individual to make a significant impact in a small organisation. Key responsibilities of the role Operational • Set the Company’s overall strategy, balancing core consulting with other activities such as personalised medicine, • Accountable for all business development and marketing activities (BDM), supporting the Head of Business Development and heads of service-lines (MIDD and Biometrics) to develop and execute on an effective BDM strategy to identify and win new business, maximise pipeline size and quality, and further grow the Physiomics brand., • Accountable for the delivery and expansion of high-quality consultancy services, supporting heads of service-lines in effective resource management to achieve excellence in consulting and develop new service capabilities aligned with growth objectives., • Accountable for general business operations, including HR and recruitment, quality, IT, business processes and management of key internal initiatives., • As required, support key client engagements, providing strategic scientific/ clinical input (depending on experience) to key projects, to ensure client satisfaction and maximise repeat business, • Ensure robust and timely management reporting and communication, including for monthly board meetings, • Liaise with NOMAD, legal advisors and the Company’s broker to ensure compliance with AIM, MAR, QCA and other applicable regulations and guidelines, • Maintain corporate policies and procedures in support of applicable corporate governance and employment regulations (e.g. share trading, GDPR, social media, anti-bribery etc), • Be responsible (together with NOMAD and broker) for the timely issuance of press releases via LSE’s Regulatory News Service where required, • Develop and communicate interim (half year) and full year annual reports to shareholders, • Set up and run the Company’s Annual General Meeting, • Set appropriate remuneration for employees, directors and officers through the Company’s board and remuneration sub-committee, including (as appropriate) bonuses and share options Candidate profile The successful candidate will be an experienced, high calibre international business executive, with an entrepreneurial spirit and evidence of driving successful growth and innovation. They are likely to have experience in delivering contract services (either as an individual or as part of a larger organisation) and a good knowledge of life sciences (for example drug development or technologies used in support of pharmaceutical R&D or clinical practice). They will be motivated to work in a small company environment where they can make a significant impact. Professional/technical experience • A proven track record of success in growing small/ medium sized service businesses or business units in life-sciences, preferably in biopharma R&D, • Extensive current client contacts across the biotech and pharmaceutical industry sector., • Prior experience of running a company or leading a team of scientific professionals within either a CRO or biopharma setting., • An understanding of the R&D process for therapeutic drug development and its challenges, • Knowledge of the international pharmaceuticals and biotechnology sector, • Strong interest in experience of working in a small company environment; willingness to roll up sleeves and get involved in a wide variety of activities, • Experience or knowledge of issues connected with running a public company helpful but not essential, • Hands-on experience in one or more of the following areas: quantitative pharmacology, clinical pharmacology, biometrics and clinical development is desirable. Qualifications • Good scientific or clinical credentials, ideally to PhD/ MD level, • Demonstrated financial acumen either through relevant experience or a qualification such as MBA Personal attributes • Self-motivated, with a readiness to take on tough challenges and see them through to conclusion, • Results focussed: Ability to set a strategic agenda and to execute to achieve long-term growth, • Good business acumen: Good understanding of the services business model and the factors to manage for successful growth, • Excellent communication skills; able to present arguments in a diplomatic, clear, concise, and logical manner, and to influence others positively, • Confidence, persona and gravitas to interface and negotiate with senior client contacts, and to confidently sell the Company’s capabilities to the outside world, • Demonstrated ability to resolve problems in a creative and positive manner and effectively maneuver through complex situations – internal and external, • A strong team leader with the flexibility to work with a wide range of skillsets and personalities consisting of the internal team, consultants, clients and third parties

Overview Pictura Bio is a well-funded University of Oxford spin-out developing a novel diagnostic platform for rapid pathogen detection. Our technology combines fluorescence microscopy with automated image analysis and machine learning to identify pathogens in seconds. The platform is being translated into clinical diagnostic products, initially focused on respiratory infections, with broader applications across infectious disease. Role Purpose You will play a hands-on role in the development, optimisation, and validation of the Pictura Bio assay. Working closely with assay development, imaging, and data science teams, you will support the transition of a research-stage assay into a robust, reproducible diagnostic workflow. This role is fully on-site and laboratory-based, and is suited to a scientist with strong experimental skills, experience in fluorescence microscopy, and an understanding of working within a quality-managed environment. You will be expected to generate high-quality experimental data, document work rigorously, and contribute to assay robustness, reproducibility, and performance verification. Major Accountabilities · Design, execute, and document laboratory experiments supporting assay development · Optimise fluorescence labelling protocols for viruses, bacteria, and other pathogens · Perform fluorescence microscopy imaging using standardised protocols · Support development and refinement of imaging workflows (sample prep, imaging parameters) · Analyse experimental data and contribute to interpretation of assay performance · Verify and validate assay performance (e.g. repeatability, sensitivity, specificity, robustness) · Maintain accurate, detailed laboratory records in line with quality requirements · Contribute to SOPs, protocols, and technical documentation · Work in accordance with company quality systems, policies, and procedures · Collaborate closely with assay, imaging, and software teams to support end-to-end assay development · Undertake other reasonable duties consistent with the role and level Ideal Background Education · BSc or MSc in a relevant discipline (e.g. Biophysics, Biomedical Sciences, Microbiology, Molecular Biology, Bioengineering) · PhD desirable but not essential Experience · Hands-on laboratory experience in assay development or bioanalytical testing · Practical experience with fluorescence microscopy (widefield, epifluorescence, TIRF, or confocal) · Experience working under a Quality Management System (e.g. ISO 13485, ISO 15189, GLP, GxP, or similar) · Experience in an industrial, translational, or regulated laboratory environment is highly desirable Skills · Strong experimental and practical laboratory skills · Good understanding of assay development principles and experimental controls · Familiarity with fluorescence labelling and sample preparation · Ability to follow and improve SOPs and experimental protocols · Strong attention to detail and excellent record-keeping · Comfortable analysing data and reporting results clearly · Familiarity with image analysis software is an advantage · Basic Python or data analysis skills are beneficial but not essential Personal Attributes · Methodical, careful, and data/quality-driven · Comfortable working in a fast-moving, early-stage company · Willing to challenge results constructively and troubleshoot experiments · Collaborative and communicative

Life Sciences Solicitor / 5 – 10+ PQE / Oxfordshire / £90-100K + DOE – A rare opportunity to join a leading UK life sciences practice, advising innovative businesses from start-ups to global pharma organisations, within a collaborative and highly ranked team – To apply please call Gemma on 020 7183 8586. JOB TITLE: Life Sciences Solicitor PQE REQUIRED: 5+ LOCATION: Oxfordshire SALARY: £90-100K DOE THE ROLE: An exciting opportunity has arisen for an experienced Commercial Solicitor to join a top-ranked life sciences team based in Oxfordshire. This specialist practice advises a broad spectrum of life sciences and technology-based clients, including biotech, biopharma, vaccines, medical devices, diagnostics, agbiotech and tech bio businesses, as well as universities, research institutes, charities and government bodies. You will undertake a wide range of commercial work including IP licensing and partnering transactions, clinical trial arrangements, research collaborations, supply and manufacturing agreements, regulatory matters, data protection issues and due diligence for corporate transactions. Working closely with senior members of a large and highly regarded commercial IP and IT team, you will play a key role in delivering strategic advice to innovative and high-growth clients operating at the forefront of scientific and technological development. THE CANDIDATE: The successful candidate will have at least five years’ post-qualification experience gained within a strong regional, City or in-house environment. You will demonstrate solid technical expertise in commercial law and have proven experience advising life sciences or technology-based businesses. Commercial awareness, enthusiasm for the sector and the flexibility to work across a varied caseload are essential. This role would suit a proactive and ambitious lawyer seeking to deepen their sector expertise within a leading specialist team. THE FIRM: This is an award-winning, Top 50 UK law firm with a strong national presence and an outstanding reputation across multiple practice areas. The firm is known for its collaborative culture, commitment to career development and strong sector focus. You will be joining one of the largest life sciences teams in the UK, consistently ranked in the legal directories and recognised for its depth of expertise and client service. PACKAGE: The firm offers a competitive salary and comprehensive benefits package, together with flexible and hybrid working arrangements. Ongoing professional development and a supportive, inclusive working environment form a core part of the firm’s culture. HOW TO APPLY: Contact Gemma at eNL on 020 7183 8586 or email with your CV, or simply call for a confidential discussion. eNL will never share your CV with a third party without your express permission. As part of our candidate care process, we aim to respond to all applications in 7 days. If you have not been contacted within this timescale, your application has been unsuccessful on this occasion. Please note our advertisements use PQE/salary levels purely as a guide. At eNL we value diversity and inclusion. We want to attract people at all levels and encourage applications from all suitably qualified candidates whatever your ethnicity, religion, age, physical or mental disability, sexual orientation, gender identity or any characteristics protected by law in the jurisdictions in which we operate.

Overview Pictura Bio is a well-funded University of Oxford spin-out developing a novel diagnostic platform for rapid pathogen detection. Our technology combines fluorescence microscopy with automated image analysis and machine learning to identify pathogens in seconds. The platform is being translated into clinical diagnostic products, initially focused on respiratory infections, with broader applications across infectious disease. Role Purpose The Clinical Validation Lead will be responsible for designing, executing, and overseeing clinical and analytical validation of Pictura Bio’s diagnostic assays. You will lead validation strategy from late-stage development through clinical evaluation, ensuring studies are scientifically robust, regulator-ready, and aligned with the intended clinical use. This role is ideal for someone with hands-on experience validating diagnostic assays in regulated environments, particularly US LDTs, but experience with FDA-cleared/approved, UK, or EU IVD pathways is also highly relevant. You will work closely with assay development, data science, regulatory, and external clinical partners. Major Accountabilities · Lead the design and execution of analytical and clinical validation studies for diagnostic assays · Define validation plans covering precision, accuracy, sensitivity/specificity, LoD, reproducibility, interference, and cross-reactivity · Ensure validation studies are aligned with intended use, clinical claims, and regulatory expectations · Oversee clinical sample selection, handling, and testing in collaboration with partner laboratories and CROs · Support validation of Laboratory Developed Tests (LDTs), particularly within the US regulatory framework · Contribute to validation supporting FDA (e.g. De Novo / 510(k)), UKCA, or CE-IVD pathways where applicable · Review and approve protocols, reports, and data summaries for internal and external use · Work with data science teams to ensure clinical performance metrics and analyses are appropriate and traceable · Interface with regulatory and quality teams to support technical files, submissions, and audits · Manage external stakeholders (clinical sites, reference labs, CROs) involved in validation activities · Clearly communicate validation strategy, results, and risks to senior leadership Ideal Background Education · PhD, MD, PharmD, or MSc in a relevant discipline (e.g. Clinical Sciences, Biomedical Sciences, Molecular Biology, Immunology, Microbiology) Experience · Demonstrated experience clinically validating diagnostic assays · Experience with assays such as immunofluorescence, molecular diagnostics, NGS / optical sequencing (e.g. Illumina), or imaging-based diagnostics · Experience developing or validating US Laboratory Developed Tests (LDTs) is highly desirable · Experience supporting FDA-cleared/approved assays (De Novo, 510(k), PMA) or UK/EU IVD pathways is advantageous · Experience working with clinical samples (e.g. respiratory samples, blood, urine, swabs) · Experience collaborating with hospital labs, reference labs, or CROs Skills · Deep understanding of diagnostic validation principles and study design · Strong knowledge of clinical performance metrics and statistical interpretation · Familiarity with regulatory and quality frameworks (e.g. CLIA, CAP, ISO 13485, ISO 15189) · Ability to translate clinical requirements into practical validation studies · Strong documentation, reporting, and review skills · Excellent communication skills, including interaction with clinicians, regulators, and executives Desirable Personal Attributes · Highly organised and detail-oriented, with a strong quality mindset · Comfortable taking ownership of complex, multi-stakeholder validation programmes · Scientifically rigorous but pragmatic in balancing timelines and regulatory expectations · Confident communicator who can explain validation decisions clearly · Comfortable working in a fast-moving, scaling diagnostics company

Business Manager – Brand New State-of-the-Art Hospital Up to £55,000 DOE + Competitive Company Benefits Oxford Want to be a key part in the opening and success of a BRAND NEW and state of the art hospital? Compass Associates are proud to have exclusively partnered with Welbeck Health Partners for the opening of their brand-new hospital, boasting 12 specialties equipped with the latest technology and world-renowned consultants dedicated to delivering the best patient experience. Capitalising on the success of their London flagship hospital, their new site will offer a wide range of medical diagnostic and same-day minimally invasive services, including heart health, lung health, digestive health, ENT, endoscopy, and neurology. This is a very exciting opportunity for an individual who wants to help to shape a growing, but established healthcare organisation. Welbeck Health Partners was founded by leading healthcare specialists from the UK and USA who shared a clear vision: to deliver better care and redefine what a healthcare organisation can be. Welbeck’s unique partnership model empowers clinicians to share in the success of the group while fostering a collaborative environment. It provides a framework for consistent patient pathways, quality assurance across partners, and smooth cross-referrals between specialties. Joining Welbeck means becoming part of a growing network of high-quality clinics and world-leading healthcare professionals. Welbeck are committed to creating a supportive, values-driven environment where their people can thrive. The company invests in its people, providing ongoing professional development, clear career progression, and the resources needed to excel. If you’re looking to be part of a purpose-led organisation that is shaping the future of healthcare while fostering a culture of respect, teamwork, and shared success, we’d love to hear from you. What is in it for you? • Paid for park and ride, • Great work-life balance, • Professional registration paid for annually, • Personal Development Plan, • 27 Days Annual Leave + Bank Holidays, • Private Medical Insurance, • Eye Care, • Annual Flu Vaccines, • Private Pension, • Season Ticket Loan / Cycle to Work Scheme, • Employee Assistance Programme, • AND a range of policies supporting health and wellbeing We are seeking an experienced and dynamic Senior Manager with exceptional interpersonal and leadership skills. This is a unique opportunity to play a key role in establishing and growing one of the most exciting developments within the Welbeck Health Partners network. You will work alongside leading consultants across multiple specialties to deliver outstanding patient care and operational excellence. As the centre develops and expands, this role offers significant scope for professional growth and the opportunity to contribute to shaping the future of premium healthcare delivery in the Oxfordshire region. The post holder will be expected to support their team, department and centre to achieve the Welbeck Values in their day-to-day work. They will provide a responsive and efficient administrative service to meet the needs of the Business. You will be an effective decision maker, who is able to prioritise their own workload whilst responding to interruptions. The post holder will be able to deal with unpredictable work patterns and proactively deal with issues without reference to others. Responsibilities: • Overall responsibility for all business functions, including budget control, operational management of patient pathways, and billing/accounting., • Line-manage the Front of House and Administration teams, including lead administrators, receptionists, billing staff, and clinical/consultant administrative teams., • Promote a patient-centred approach, upholding exceptional customer service principles throughout the patient journey., • Ensure all staff are appropriately inducted, trained, and supported with the necessary resources to perform effectively., • Identify and address training and development needs for staff, ensuring performance appraisals and development plans are completed in line with policy., • Recruit suitable candidates for Front of House, Administration, and clinical support roles as required., • Support the Centre Director, Clinical Service Director and Operations Director in identifying new business opportunities, service redesign initiatives, and operational improvements focused on patient care., • Use service improvement techniques, audit processes, and data analysis to monitor and enhance service delivery., • Engage proactively with service users, clinical teams, and key stakeholders to ensure feedback informs service planning and continuous improvement., • Assist in implementing and maintaining clinical governance, complaints, and risk management processes, monitoring compliance with regulatory standards and best practice., • Support clinical staff in root cause analyses of complaints, incidents, and operational issues, ensuring timely resolution and learning., • Collect, interpret, and report on data relating to service performance, patient satisfaction, and operational efficiency, recommending corrective actions as necessary., • Ensure appropriate administrative and operational coverage in line with service needs, including contingency planning., • Oversee debt collection reporting and management, working with internal teams and external agencies to optimise financial performance., • Adopt a data-driven approach to decision-making to improve services objectively and effectively., • Develop and maintain effective communication channels across teams to foster collaboration, engagement, and a high-performing work culture, • Ensure compliance with HR, health & safety, and regulatory requirements across all business functions., • Champion a culture of continuous improvement, innovation, and operational excellence throughout the service. Recommendations We’re currently recruiting for a variety of management, clinical, and non-clinical roles across Oxford and Cambridge. If this role isn’t for you but you are interested in exploring other opportunities, feel free to share your details. If you know someone who may be interested in this or other roles in a new private hospital, we offer a £200 voucher referral reward for every successful recommendation.

CPL Life Sciences are proudly partnering with an early-stage biotech developing novel therapies and are looking for a Clinical Project Manager to help drive the delivery of early phase clinical trials. This is a great opportunity for someone who thrives in a fast-moving biotech environment, enjoys taking ownership of studies, and is comfortable wearing multiple hats while supporting a growing clinical operations team. You will oversee the operational delivery of Phase II clinical studies, working closely with internal teams, CRO partners, and investigative sites. The role also includes mentoring Clinical Trial Assistants (CTAs) and helping shape clinical operations processes as the company grows. Key responsibilities: • Lead the day-to-day operational management of Phase II clinical trials, • Oversee CROs, vendors, and site relationships, • Manage timelines, milestones, and study deliverables, • Identify operational risks and implement mitigation strategies, • Ensure compliance with ICH-GCP and regulatory requirements, • Support study documentation and clinical trial planning, • Mentor and support Clinical Trial Assistants within the team, • Collaborate cross-functionally with clinical development, regulatory, safety, and data management Key experience required: • Experience managing clinical trials within biotech or pharma, • Strong understanding of clinical operations and ICH-GCP, • Experience supporting or mentoring junior clinical team members (e.g. CTAs), • Proven ability to manage vendors and CROs, • Comfortable working in an early-stage biotech environment with a hands-on approach, • Adaptable, collaborative, and solutions-focused Hybrid working in Oxford- flexible on a weekly or bi-weekly basis.

Applied AI Scientist / AI Engineer AI & Robotics Division | Oxford Onsite Requirement- x2 days per week A rapidly growing global research and technology institute is expanding its Applied AI division, growing from ~100 to ~200 employees over the next year. The team focuses on translating cutting-edge AI research into real-world impact across healthcare, climate, food security, robotics, and advanced materials. Unlike pure research groups, the Applied AI team works directly with scientists and collaborators to define problems, build models and pipelines, and deliver usable solutions. The group collaborates closely with Data Engineering and Infrastructure teams to deploy scalable AI systems. Key Focus Areas • Health foundation models (DNA / patient journey modelling), • Autonomous Labs – ML, vision, sensors, and robotics to automate lab workflows, • Applied partnerships in vaccines, clinical modelling, plant phenotyping, and materials research We’re Hiring Applied AI Scientists and AI Engineers across multiple levels, with interest in: • Computer Vision (3D reconstruction, sensor systems), • Protein / DNA modelling, • LLM engineering with production deployment Candidates should be comfortable building robust ML pipelines and scalable systems, working closely with domain experts, and delivering practical outputs for scientific users. Teams work in cross-functional groups, with core in-person collaboration days twice per week.

Immunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company whose purpose is to develop and commercialize a new generation of transformative medicines which address unmet patient needs in oncology, infectious diseases and autoimmune disease. Our leaders in R&D are internationally recognised as some of the biotech industry's most successful drug developers. We are creating not just an environment where great minds can interact but an innovation powerhouse answering the big questions. Focused on delivering first-in-class biological therapies to patients, we have developed a highly innovative soluble TCR platform. Our ImmTAX molecules underpin a new generation of precision engineered drugs that harness the immune system to treat a broad spectrum of diseases with high unmet medical need, including oncology, infectious diseases and autoimmune diseases. At Immunocore, we recognize that our employees are our greatest asset. We value the unique contributions each person brings to our team. By embracing Science, Trust, Respect, Integrity, Diversity, and Entrepreneurship (STRIDE), we create an environment where collaboration thrives, ideas flourish, and transformative changes happen. STRIDE represents more than just letters; it embodies our shared identity and drives our mission. We are dedicated to developing breakthrough therapies that transform patients' lives, advancing medicine, and supporting one another in these pursuits. Immunocore is proud to be an equal opportunity employer. As such, we are committed to fostering an inclusive workplace where everyone feels valued, respected, and empowered. We encourage applications from individuals of all backgrounds, regardless of race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, or any other characteristic protected by law. To characterise the companies biotherapeutic recombinant T-cell receptor based and related molecules using a wide variety of protein characterisation and mass spectrometry methods. To contribute to the development of characterisation methods for the company's biopharmaceutical products, including peptide mapping (LC-MS/MS) and intact mass spectrometry analysis. KEY RESPONSIBILITIES • Supporting drug substance and drug product impurity characterisation and identification, • Performing protein sequence and post translational modification identification, including glycosylation analysis., • Supporting drug substance and drug product process development by performing characterisation of process intermediates, • Contribute to the Development of characterisation methods of ImmTAX and other products, including peptide mapping (LC-MS/MS) and intact mass analysis, • Designing and carrying out biochemical characterisation, chemical stability and comparability studies of biologics/drug products., • Contribute to writing study protocols and reports., • Independently testing and, increasingly, leading lines of investigation. Proposing new experiments based on emerging data and other related information. Providing support on technical aspects to others., • Priorities: establishing priorities for own work and team-based projects; making decisions on prioritisation based on the overall goals of the team, department and project, using direct evidence and personal experience as guidance., • Technical Knowledge: sharing knowledge with the wider team and, across departments representing the department. May also act as a mentor to other colleagues, sharing scientific knowledge. Providing analysis of new techniques and theories from outside the Company to advance the way the company works; sharing these with leaders across the department., • Laboratory records: ensuring that all records and information are up to date, on time and recorded to the correct standard. Supporting and encouraging others to achieve this., • Laboratory equipment: providing technical guidance to others within the team on how to use equipment most effectively., • Reporting: communicating and presenting research findings at meetings with colleagues, senior management and partners., • Adhere to safe working practices in laboratories according to Immunocore EHS policies. PERSON SPECIFICATION Experience & knowledge Essential • Experience in development of HPLC based peptide mapping methods and mass spectrometric characterisation of recombinant proteins or antibodies., • Experience of glycosylation analysis of recombinant proteins or antibodies., • Independently coordinated extensive testing of protein biomolecules., • Experienced in the characterisation of proteins expressed in both microbial and mammalian systems., • Understanding of expected post-translational modifications in biological systems., • Worked in a bench-based biopharmaceutical laboratory environment., • Experienced in assay development, • Familiar with biopharmaceutical stability study principles and interpretation thereof, • Worked and contributed actively in a diverse team environment, • Proposed and driven changes in working practices that have improved efficiency, supported teams through adoption and change, • Presented detailed scientific findings and papers to internal and external audiences Desirable • Experience of glycosylation analysis of recombinant proteins or antibodies, • Experience with late stage/commercial biopharmaceutical assay development and characterisation, • Familiar with the principles of Good Manufacturing Practise (GMP), • Presented at external conferences, • Led a small project team, formally or informally, through a change in practice including project management, • Understanding of analytical requirements to support materials for use in clinical trials Education & qualifications • Essential: BSc. Or MSc. in biochemistry, biotechnology or related discipline, • Desirable: PhD in related discipline

Immunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company whose purpose is to develop and commercialize a new generation of transformative medicines which address unmet patient needs in oncology, infectious diseases and autoimmune disease. Our leaders in R&D are internationally recognised as some of the biotech industry's most successful drug developers. We are creating not just an environment where great minds can interact but an innovation powerhouse answering the big questions. Focused on delivering first-in-class biological therapies to patients, we have developed a highly innovative soluble TCR platform. Our ImmTAX molecules underpin a new generation of precision engineered drugs that harness the immune system to treat a broad spectrum of diseases with high unmet medical need, including oncology, infectious diseases and autoimmune diseases. At Immunocore, we recognize that our employees are our greatest asset. We value the unique contributions each person brings to our team. By embracing Science, Trust, Respect, Integrity, Diversity, and Entrepreneurship (STRIDE), we create an environment where collaboration thrives, ideas flourish, and transformative changes happen. STRIDE represents more than just letters; it embodies our shared identity and drives our mission. We are dedicated to developing breakthrough therapies that transform patients' lives, advancing medicine, and supporting one another in these pursuits. Immunocore is proud to be an equal opportunity employer. As such, we are committed to fostering an inclusive workplace where everyone feels valued, respected, and empowered. We encourage applications from individuals of all backgrounds, regardless of race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, or any other characteristic protected by law. The primary purpose of this role is to contribute to cross functional efforts focused on applying the ImmTAX® platform or other modalities to the development of novel treatments for chronic infections, including HIV and HBV and EBV-associated diseases. The team is involved in multiple stages of the drug discovery and development process, from target discovery all the way to clinical trials. Examples of key preclinical research are published in Yang H et al., Mol Ther. 2016; 24,11; Fergusson J et al., Hepatology 2020; 72,5; Wallace Z et al., Mol Ther 2024; 32, 678. The postholder will plan, design and execute experimental investigations to support the advancement of the Company pipeline, processes and technology capabilities, with guidance from their manager, ensuring that project goals are met within time and budget constraints. They will be expected to demonstrate technical proficiency, rigour in assessing their own data and that of others, scientific creativity and independent thought. This position requires participation and presentation of results at internal meetings, sharing information learned at external scientific meetings and establishing productive relationships with colleagues across Research and other departments. Key Responsibilities: • With instruction and guidance from manager - plan, design, and execute assignments to meet project goals within defined timeframes, • Execute experiments to address key scientific questions and enable project progression, utilizing range of molecular and cellular techniques including some of the following: NextGen sequencing, DD-PCR, qPCR, cell culture, flow cytometry, ELISpots, ELISAs,, • Some work will be conducted in a containment level 3 (CL3 facility) and will require handling of human viruses, • Analyse data, interpret results, and make recommendations, • Proactively expand scientific/technical knowledge in relevant fields including HIV/HBV/EBV related disease biology and drug development through review of scientific literature/ conference updates, peer to peer mentoring, and attendance at seminars/conferences in line with company strategy, • Work effectively in a matrixed team structure and as part of cross functional teams, • Participate and present results at internal meetings, • Establish relationships and possible collaborations within and outside of the company Education, Experience and Knowledge: Essential Qualifications: • PhD in molecular biology, cell biology, genomics, virology, immunology, or related discipline and 0-2 years related experience, • Alternatively, a BSc or MSc with significant work experience in relevant scientific areas Preferred Qualifications: • Knowledge/expertise of Immunology/HIV/HBV/EBV, • Flow cytometry, ELISAs, ELISpots, • Viral integration site analysis

I am looking for a Mobile Occupational Health Technician to join an expanding peripatetic team. In this role, you will be required to travel across the UK, driving a Mobile Medical Unit (MMU) to client sites to deliver high-quality health surveillance services. This is a varied and rewarding role that plays a vital part in ensuring the health and wellbeing of employees across a range of industries. This is a great opportunity for an enthusiastic and reliable individual to expand their skills and experience in a supportive environment, where you’ll be given a 3-week Training and Induction Programme with ongoing mentoring and support from the team. You will: * Conduct health surveillance screenings, including audiometry, lung function testing, and baseline measurements such as height, weight, blood pressure, and urinalysis. * Accurately record all medical information in occupational health records and ensure it is passed to the relevant clinical staff. * Maintain and ensure all equipment is clean, serviceable, and fit for purpose. * Support health promotion activities and other additional tasks as required. * Assist the wider occupational health team by gathering and recording accurate information to support clinical decision-making. * Provide biometric data through screening procedures to enable nursing and physician staff to make informed clinical decisions regarding patient management. You will be a high...

Occupational Health Technician Location: Oxford (with occasional UK travel) Salary: £25,000 – £27,000 per annum (depending on experience and qualifications) Hours: Full-time, 37.5 hours per week (typically between 8am – 6pm) A leading occupational health provider is seeking a motivated and professional Occupational Health Technician to join its expanding peripatetic team. This role offers the opportunity to make a real impact on workplace wellbeing while travelling across the UK to deliver high-quality health surveillance and screening services to a wide range of industries. Based in Oxford, the successful applicant will drive a Mobile Medical Unit (MMU) to client sites, carrying out essential health assessments and ensuring the safety and wellbeing of employees, with the occasional travel nationwide. Key Responsibilities: • Conduct a range of health surveillance and screening activities, including audiometry, lung function testing, and baseline measurements such as height, weight, blood pressure, and urinalysis. • Accurately record medical information in occupational health records and share findings with relevant clinical staff. • Ensure all medical equipment is clean, calibrated, and fit for purpose. • Support health promotion initiatives and assist in additional occupational health duties. • Provide accurate biometric data to assist nursing and physician staff with clinical decisi...

Are you a Solicitor with a passion for the Life Sciences sector? At our award-winning law firm, your expertise will be nurtured, your career growth championed, and your contributions valued. Step into a supportive environment where you can grow with us. The role We are looking for a senior commercial solicitor to be based in Oxford, to undertake a wide range of work for our life sciences clients and other technology-based clients. Our life sciences team is one of the largest specialist sector practices in the UK and advises businesses ranging from start-ups and fast growing developing businesses to large multinationals (e.g. global pharma and medtech organisations), as well as universities, research institutes, medical research charities and government organisations. We advise life sciences businesses across the full sector spectrum, including in relation to biotech, biopharma and vaccines, medical devices and diagnostics, tech bio and agbiotech. As part of our top-ranked team, you will be working with our head of life sciences James Fry, as well as other members of our large and friendly commercial IP and IT team. The person You will have 5+ years post qualification experience gained in a large regional or City firm, or in-house. You will have good technical skills in commercial law and proven experience with life sciences businesses. You will be an enthusiastic and commercially-minded lawyer prepared to turn your hand to a wide range of work. The work Advising on: • IP licensing and partnering transactions, • clinical trial arrangements, • research collaborations, • promotional arrangements, • other commercial contracts (including supply and manufacturing transactions), • IP advisory and protection, • regulatory issues in life sciences, • data protection The benefits As you'd expect, we offer a competitive salary and a wide range of benefits. ___ to find out more about our core benefit offering. Pre employment screening If we offer you a role, we will conduct comprehensive pre-employment screening. This screening will include, but is not limited to, a basic DBS, verification of your right to work, a three year employment history and a self-declaration to assess your character and suitability for the role. Full details of our pre-screening employment process are available upon request. The firm Mills & Reeve is centred on achieving more for clients, their businesses and the wider communities we serve. Our clients and their industries benefit from our knowledge and learning, and receive consistent experiences with no surprises. We tell them what they need to know when they need to know it. We build personal relationships, with advice individually tailored to individual need. And if clients need things we don't offer, we draw on our network to give recommendations. Our 1,250 plus people and over 750 lawyers share one vision - achieving more for clients. By joining Mills & Reeve, you'll have the chance to build your skills and experience within a firm that's not only ranked in the top 50 UK law firms, but also one that truly values their people. Our mantra is "Achieve more. Together.", which we feel embodies our purpose and is more than just a catchphrase! We're also ranked in the Sunday Times Best Places to Work list, and were recently awarded Platinum Investors in People. and finally Everyone at Mills & Reeve brings a unique perspective and ideas to the team and we do everything we can to help each person to thrive. We're committed to providing an inclusive and supportive working environment, are happy to consider flexible working arrangements, and want to achieve the right balance for both our people and the firm. We encourage everyone to ask if they feel they need any workplace adjustments, and will do our best to support with these. To find out more about our diversity and inclusion work, ___. Documents

Responsible for budget management for the Dental Services and for monitoring income, expenditure and activity data transmission to the NHS Business Services Authority (BSA) in relation to patient care. Additional Information We are looking to recruit a Clinical Director to lead the Oxfordshire Commu

A healthcare data solutions company based in Oxford is seeking a Clinical Data Scientist to enhance patient care through valuable real-world data. This role requires a medical degree and experience in NHS data, as the candidate will collaborate with teams to improve data quality and informatics proj

A leading healthcare research firm in the UK is seeking an Oncology Clinical Researcher to design and manage oncology clinical trials. This remote role involves ensuring trial data meets real-world standards and translating outcomes into regulatory reports. The ideal candidate has significant experi

As a member of the Informatics team, you will work closely with Engineering, Machine Learning and Real-World Evidence (RWE) teams, as part of the data platform product group, and will support and collaborate with Data Strategy and Partnerships team on identifying appropriate data sources, design aut

Blue Earth Therapeutics is a clinical‑stage radiopharmaceutical company developing the next generation of precision radioligand therapies for cancer. With a strong leadership team, cutting‑edge science, and an exciting growth trajectory, we are expanding our CMC & Supply Chain function with the addition of a highly organised and proactive CMC & Supply Chain Associate initially on a 6 month FTC. This is an excellent opportunity for someone looking to develop within radiopharmaceuticals, clinical supply, and logistics while playing a crucial role in delivering therapies to patients across Europe and the USA. The Opportunity As our CMC & Supply Chain Associate, you will support the end‑to‑end supply of therapeutic radiopharmaceuticals for multiple clinical studies. Working closely with the Supply Chain Manager, cross‑functional teams, and key external partners, you will help ensure the seamless flow of materials, documentation, and operational processes. Your work will directly contribute to ensuring patients receive high‑quality therapeutic doses on time — a pivotal role in our mission to deliver targeted radiotherapies that make a genuine difference. Key Responsibilities Support the full supply chain process, ensuring documentation and critical steps are completed accurately and on schedule Manage inventory, including retest/expiry oversight, and coordinate shipment of key materials (e.g., isotope, precursor) Raise quality‑related issues with QA and Supply Chain teams Maintain accurate records of supply, expenses, and clinical product usage Become an SAP user for PO raising, goods receipting, and invoice processing Keep organised, compliant, contemporaneous records of manufacturing and supply Conduct batch data trending and assist with operational metrics Organise internal and external meetings, vendor calls, and take minutes Support preparation of presentations and project materials Ensure compliance with the company Quality System and pharmacovigilance expectations Participate in ongoing professional development About You A scientific degree or relevant experience in a similar role Experience with radiopharmaceuticals or supply chain/logistics (desirable) Experience or understanding of EU GMP principles (desirable) Strong organisational and prioritisation skills Thrives in a dynamic, fast‑paced environment Proficiency in Microsoft Excel, Word, and PowerPoint A proactive, flexible team player with excellent attention to detail Good verbal and written communication skillsWhy Join Blue Earth Therapeutics? At Blue Earth Therapeutics, you'll be part of an ambitious, fast‑growing company at the forefront of radioligand therapy. We offer: A highly collaborative, supportive culture Opportunities for personal and professional growth A clear link between your work and real patient impact Competitive salary and benefits A team that celebrates milestones and innovates togetherIf you're driven, motivated, and excited by meaningful work in a rapidly advancing field — this role is for you

Shape the Future of Healthcare Infrastructure at Oxford Health Are you a precision-focused professional with a passion for quality and safety? Oxford Health NHS Foundation Trust is looking for a Clerk of Works to become the eyes and ears of our Capital Development team. In this role, you aren’t just "inspecting buildings"—you are ensuring that our clinical environments are safe, compliant, and built to the highest standards for the patients and staff who rely on them every day. Why This Role is Different • Total Project Oversight: You will follow projects from RIBA Stage 3 all the way through to final handover and the 12-month warranty sign-off.., • Influence & Quality: You have the authority to witness commissioning, identify defects, and verify that every material used meets our exacting standards.., • A Collaborative Environment: Work alongside contractors, architects, and clinical leads to solve complex problems and ensure smooth "soft-landing" handovers.., • Autonomy with Support: We value your ability to set your own agenda and work proactively, backed by the leadership of the Head of Capital Development Main duties of the job Your Impactful Day-to-Day • On-Site Leadership: Conduct regular inspections, monitoring trade staffing levels and site progress against the master programme., • Safety Stewardship: Maintain the highest safety standards by issuing Permits to Work and auditing contractor safety systems., • Problem Solving: Identify new risks, contribute to the Project Risk Register, and recommend corrective actions to keep projects on track. Who You Are • Experienced & Qualified: You hold a relevant construction or engineering qualification (like an ONC/OND) and have a background in site project management., • Safety-Minded: You have an IOSH in safety management and a rock-solid understanding of construction regulations., • An Expert Communicator: You can distill complex technical data into clear reports for various audiences, from professional bodies to the public., • Adaptable: You thrive under pressure, managing multiple projects simultaneously while maintaining meticulous attention to detail., • Financial Integrity: Help keep projects on budget by verifying contractor invoices and extra-work instructions.. Working for our organisation Oxford Health is a great place to work and to be able to showcase the best of yourself when making an application please read the “candidate guide to making an application” and ensure your supporting statement is tailored to the role you are applying for and addresses any essential criteria. As a Trust we provide physical, mental health and social care for people of all ages across Oxfordshire, Buckinghamshire, Swindon, Wiltshire, Bath and Northeast Somerset. Our services are delivered at community bases, hospitals, clinics and people’s homes, delivering care as close to home as possible. Our vision is that no matter who you are or where you are, you will tell us that you receive: “Outstanding care delivered by an outstanding team” Our values are: “Caring, safe and excellent” We offer a wide range of benefits designed to support your career and wellbeing. These include: • Excellent opportunities for career progression • Access to tailored individual and Trust wide learning and development • 27 days annual leave, plus bank holidays, rising to 33 days with continuous service • NHS Discount across a wide range of shops, restaurants and retailers • Competitive pension scheme • Lease car scheme • Cycle to work scheme • Employee Assistance Programme • Mental Health First Aiders • Staff accommodation (please note waiting lists apply) • Staff networking and support groups hosted by our Equality, Diversity & Inclusion team

Working closely with the Project Manager and Science Lead, the Associate Clinical Data Manager will be responsible for data cleaning and transfer of clinical neuroimaging data on a varied portfolio of neurology clinical trials. The Associate Clinical Data Manager will be the escalation point and poi

Ambition to develop professional clinical and research skills. Are you a physiologist or biomedical scientist with a passion for clinical and translational research? We have an exciting opportunity for a highly skilled, motivated and enthusiastic individual to join our established anaesthetics resea

The successful candidate will manage clinical trials, collate research data, and collaborate with multidisciplinary teams to enhance research protocols.

A prominent educational institution in Greater London is seeking an Assistant for the Clinical Laboratory. In this role, you will handle the sorting and dispatching of lab test reports, input essential data, manage sample collection, and maintain accurate records.

General knowledge of clinical trial processes and/or experience working with clinical data. Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Reviewer to join our Global Clinical Coding & Support team. Comprehensive manual review of cl

A healthcare organization is seeking a committed pharmacy technician to lead clinical trials at an innovative clinical research facility. Candidates should hold post-registration training in hospital pharmacy with relevant clinical trials experience.

Clinical Data Reviewer (UK Only - Remote). The CDR may be responsible for the clinical data review of one or more studies with the ability to move easily from project to project as necessary. In addition the CDR ensures data readiness for important milestones including, but not limited to, interim a

This role involves supporting clinical trials, providing patient‑centred services, and ensuring compliance with Good Manufacturing Practice.

The ideal candidate will possess an accredited Clinical Coding Qualification and demonstrate strong analytical skills and attention to detail. A leading healthcare provider in Greater London seeks a motivated Clinical Coder to join their team. In this role, you will extract and analyze clinical info

The Senior Data Manager brings advanced understanding of the clinical data management process from study start-up through database lock, including database design and data validation as per the requirements in the clinical study protocols, data review plan, and data management plan, and oversees the

Have knowledge of database structure and data management techniques,. Collaborate with the project team on the overall data management strategy for the program or project to ensure overall quality and efficiency. Lead the development of CRF specifications, validate them, and conduct editorial review

Curate, validate and reconcile clinical data with laboratory/biomarker and study datasets; resolve data queries with clinical teams. Your primary responsibility will be to systematically extract and curate clinical data from medical records (electronic patient record systems and, where applicable, p

Data Management plan (DMP), Data Validation Plan (DVP), Data Entry Guideline, Database Specification Document (DBSD), Database Report (DBR)) in the DM TMF. Provide validated data exports from the EDC system or the clinical database to authorized recipients (e. Combine external data with the clinical

The role involves managing data processing activities, leading projects, and ensuring compliance with clinical trial regulations. Candidates should have a bachelor's degree in health or pharmaceutical sciences, with a minimum of 2 years of experience in clinical trial data management. A leading CRO

A leading medical provider in York is seeking an individual to handle administrative and coding tasks, ensuring the efficient management of patient records and supporting GPs to deliver quality care.This role involves 30 hours of work per week, Monday to Friday.The ideal candidate will prioritize pa

In this vital role, you will support the clinical research team with administrative duties, ensuring compliance with Good Clinical Practice (GCP). A leading cancer care institution in Greater London is seeking a Clinical Trial Administrator. We're looking for candidates with clinical research experi

We’re looking for a Group Product Manager – Clinical Data & Monitoring Technologies to join our Product Management group and contribute to our mission of transforming clinical research through data‑driven insights. This individual will bridge clinical data operations with product management, l

The Senior Data Manager brings advanced understanding of the clinical data management process from study start-up through database lock, including database design and data validation as per the requirements in the clinical study protocols, data review plan, & data management plan, and oversees the c

This role requires extracting and validating clinical data from medical records, integrating this data into research repositories while ensuring its quality and completeness. A leading UK university seeks a Clinical Research Data Integration Coordinator to work on cancer research initiatives. The id

A leading technology firm in the UK is hiring an AI Engineer to build AI-powered solutions for clinical data processing.

A leading biopharmaceutical solutions organization is seeking a Clinical Data Reviewer to take responsibility for the clinical data reviews of relevant studies. The ideal candidate will use their comprehensive knowledge of therapeutic areas to ensure data validity and readiness for milestones.

As the Vice President, Data Management, you will be responsible for the strategic leadership, delivery, development, and oversight of the global Data Management department. They act as an executive oversight, ensuring delivery execution and leading teams with a goal of real-time, efficient data flow

A clinical research organization is seeking a Clinical Data Manager to lead data processing and management activities for clinical trials. This role requires a Bachelor's degree and at least 2 years of experience in clinical trial data management. You will be responsible for managing timelines, ensu

Data Validation & Quality Control: Take responsibility for the execution of data validation activities to ensure data consistency, accuracy, and completeness, EDC checks, datalists and other data review tools to ensure data integrity. Data ManagementStudyParticipation: Conduct all clinical data mana

A healthcare organization based in Greater London is looking for a Divisional Research Nurse to support a diverse portfolio of clinical research studies including neurological conditions. Essential qualifications include being a Registered Nurse, along with relevant experience in clinical trials.

A leading healthcare provider in Greater London is seeking a Clinical Auditor for its ADHD services to improve patient care through clinical audits and data analysis. The successful candidate will have clinical healthcare qualifications, at least five years of experience, and a commitment to enhanci

A full-service clinical contract research organization in Greater London is seeking an experienced informaticist to lead advanced analyses and create predictive data models.