Jobs in Oxford England Uk

Product Manager

From $10/yr

At ONI, we are driven by a profound mission: to propel scientific discovery and combat diseases by granting everyone the ability to visualize, comprehend, and share the intricate microscopic details of life. Our revolutionary Nanoimager and Aplo Platform stand at the forefront of advancing cellular studies on a molecular level, making substantial contributions to the evolution of scientific knowledge. We’re looking for a Product Manager to own our kits and workflows, including EV Profiler and LNP Profiler, now that the concept is proven. You’ll make sure sample preparation, fluid handling, imaging, analysis and reporting software work together as one system, and your responsibility is the complete customer experience, from sample to scientifically meaningful result. The job is making that system rock solid: hardening what’s already on the market, making sure it works the same way at every site, and getting more customers on it without support load growing at the same rate. The Role As part of the Product team, you’ll own the product management of our kits and end-to-end workflows, including the Discovery Kit, EV Profiler and LNP Profiler and their future revisions. You will ensure these work together with automated sample preparation and fluid handling, imaging, analysis and reporting software to deliver reliable, reproducible and intuitive solutions for our customers. The initial products have launched, and the work now is making them dependable, repeatable, and scalable for our customers. You’ll create clarity and momentum for the R\&D teams by understanding which problems matter, turning customer and market evidence into priorities, and removing barriers to delivering a coherent solution. You’ll grow adoption to routine use across many sites, including bioprocessing and QC settings where results must be reproducible and defensible, and you’ll work with Marketing on positioning and the product story as the portfolio evolves. You will play a critical role in bringing these quality improvements to the market and ensuring that current and future kits maintain their quality over time, and you’ll help define the roadmap for next iterations of existing and future kits and workflows. As a product manager, you’ll be the connective tissue between software, hardware, bioware, support, and the field, acting as the voice of the customer to help internal teams better understand our customers’ needs and problems. The role is ideal for a technically curious, commercially aware individual who loves getting hands-on with products, takes ownership of outcomes and thrives on complex, cross-functional challenges. You will work broadly across our platform and alongside US colleagues; the position is based in Oxford and involves occasional travel to customers and our US team (typically 10-20%). What you’ll do * Understand scientists and their complete workflows first-hand. Work with customers and field teams, study usage and support data, and synthesize their sometimes conflicting inputs into the problems worth solving. * Drive evidence-led product direction and priorities across our solutions with R\&D and commercial leaders, balancing customer outcomes, differentiation, adoption, reliability, margin and technical feasibility. * Own the roadmap for our kits (including the Discovery Kit and the EV and LNP Profiler kits) and workflows, balancing quality, reliability, usability and new features. * Identify and prioritize the right customer and market problems, document them as clear market requirements, product performance requirements and user stories, and give development teams the context they need to design the best end-to-end solution—from sample preparation in Aplo Flow, through acquisition in Aplo Scope, to analysis in CODI. * Own validation for each kit and workflow: define acceptance criteria, performance specifications and validation plans, including reference samples and reproducibility across instruments, operators and sites. Work with R\&D, who own development and verification. * Become a hands-on power user of the full integrated workflows, from the manual and automated sample preparation of kits, imaging, analysis and reporting, identifying points of friction in the overall user experience. * Drive coherence across our end-to-end solutions, ensuring kits, reagents, lab automation, instruments and software evolve together rather than as disconnected products. Champion reproducibility, usability and reliable results across the complete workflow. * Connect R\&D, operations, quality, service, field applications, sales, marketing and customers. Establish feedback loops, clear ownership and effective cross-team decisions across our teams in the US and the UK. * Own pricing and packaging for our kits and workflows, balancing customer value, competitiveness and margin targets. * Work with Marketing throughout a product's life to shape positioning, the value proposition and the product story as the portfolio evolves, not only at launch. * Lead launch and release planning with R\&D and Marketing: set readiness criteria, make go/no-go decisions, and coordinate documentation, release notes and training for each launch or revision. * Create and run webinars and internal training for the field application and sales teams on new products and revisions, and keep an accurate record of what each kit, instrument and software version can deliver. * Track post-launch performance, including adoption, kit reorders, time to first result, reproducibility, support burden, customer feedback and commercial results, and use it to set priorities. * Help investigate and reproduce difficult issues, equip support and field teams with workarounds and guidance, and bring well-evidenced problems to developers. Analyze tickets, logs and customer feedback to find recurring failure modes, and prioritize root-cause fixes into the roadmap. * Work with Quality and Operations on manufacturing transfer, life cycle support and end of life, so our kits and workflows maintain quality over time. * Maintain broad portfolio knowledge across all of ONI’s products and use cases, while maintaining primary focus on our integrated workflows. What you’ll bring * A life-science background, ideally EVs, LNPs, nanoparticle characterization, imaging or biophysics. Being able to speak the language of our customers is critical. An MSc/PhD or equivalent hands-on experience is a real plus. * Fluency across software, instruments, laboratory workflows and multidisciplinary R\&D; comfortable investigating issues hands-on and understanding how the system fits together. * Experience working with empowered, cross-functional development teams: knowing when to provide context, decide on a trade-off and leave the solution to specialists. * Product management (or product owner) experience in life-science tools or instrumentation, ideally taking something from first release to a scaled, supported product. * Experience planning and running launches with Marketing, R\&D and the field, from development through adoption. * Commercial and pricing judgement: You can weigh customer value, competitiveness and margin when setting price and packaging. * A quality mindset: You’re comfortable writing acceptance criteria and test plans, and you think about risk, reproducibility and traceability. Exposure to a quality system (ISO 9001 or 13485) is a plus. * Comfort with data: logs, tickets, precision and method-comparison numbers (CVs, site to site). Evidence sets priorities, not the loudest voice. * The ability to lead across software, hardware, bioware, support and field without owning any of them, and to prioritize when everything feels urgent. * Clear writing and organization skills. Requirements, release notes and docs that other people can act on. Nice to have * Super-resolution or single-molecule imaging experience (dSTORM, PALM, DNA-PAINT), or general microscopy experience (TIRF, widefield, confocal, spinning-disk). * Hands-on EV or LNP work in research, biopharma, gene therapy or drug delivery. * Laboratory automation, automated liquid handling, sample preparation, consumable kits, workflow integration, scientific software or data analysis. * Integrating instruments, software, consumables and automated lab workflows; exposure to verification, validation, quality systems or lifecycle support. * Commercialization, pricing, segmentation, product positioning or product marketing in technically sophisticated markets. At ONI, we understand that a fulfilling career involves more than just challenging work - it's about enjoying a well-rounded experience. When you become a part of our team, you not only contribute to groundbreaking research but also enjoy a range of benefits designed to enhance your life both inside and outside the workplace. As an equal opportunity employer, we prioritize fairness and respect, ensuring every team member thrives regardless of their background. But that's not all - our perks include: Competitive Compensation We recognise and reward your talent. Enjoy a competitive salary that reflects your expertise and contributions, ensuring your hard work is recognized. 28 days of annual leave plus local bank holidays and 4 dedicated wellbeing days. Private Healthcare and Dental Coverage: Your health matters to us. Access top-notch medical and dental services, ensuring your well-being is in good hands. Inclusive Culture: Be a valued member of our diverse, inclusive family. Your unique perspective is celebrated here, fostering a culture of mutual respect and understanding. Health Assured: Your mental health is essential. Access our comprehensive mental health support services for a balanced work-life experience. People’s Pension: Secure your future with our pension scheme, investing in your financial well-being beyond the workplace. Perks at Work: Enjoy exclusive discounts and deals through our perks at work program, adding value to your everyday life.

Associate Director, R&D Ethics & Compliance

Department: R\&D Quality, Ethics \& Compliance Location: Oxford, United Kingdom Your impact begins here As the principal Ethics \& Compliance advisor for Novo Nordisk R\&D UK, you will have the opportunity to build and lead the compliance programme for our UK R\&D site. Working at the intersection of science, regulation, and responsible business, you will shape the governance that enables R\&D teams to make confident, well-informed decisions. Your expertise will connect UK and European regulatory and industry code of practice requirements with Novo Nordisk’s global standards. In doing so, you will help ensure that our interactions with healthcare professionals, healthcare organisations and patient organisations are lawful, ethical and built on trust. What You’ll Bring You are an experienced pharmaceutical Ethics \& Compliance professional who can combine regulatory expertise with sound judgement, pragmatism and a strong business focus. You are comfortable advising senior leaders, challenging constructively and influencing decisions across a complex matrix organisation. You Will Bring * A relevant degree in Law, Medicine, Pharmacy or an equivalent discipline, together with a foundational qualification in data privacy. * Detailed knowledge of UK and European pharmaceutical law, the Association of the British Pharmaceutical Industry Code of Practice, European Federation of Pharmaceutical Industries and Associations standards, Medicines and Healthcare products, Regulatory Agency guidance and data-privacy regulation. * Substantial pharmaceutical-industry experience leading or advising on complex compliance matters at a senior level. * The ability to influence without direct authority and build alignment across global and cross-functional teams. * Strong analytical, project leadership and stakeholder-management skills. * Confidence presenting to directors and senior leadership, as well as delivering effective compliance training both online and face to face. Experience reviewing promotional and non-promotional materials against the Association of the British Pharmaceutical Industry Code of Practice is considered an advantage. What You’ll Do * Build, implement and oversee the Novo Nordisk R\&D UK Ethics \& Compliance programme, covering UK medicines law, industry standards, data privacy and relevant artificial intelligence requirements. * Establish and drive the Novo Nordisk R\&D UK Ethics \& Compliance Governance Committee, creating a clear forum for oversight, decisions and accountability. * Advise colleagues and senior managers on complex regulatory and compliance matters, translating requirements into practical, proportionate guidance. * Lead the development of standard operating procedures, compliance risk management and corrective action plans arising from audits or complaints. * Establish effective transfer-of-value processes for interactions with healthcare professionals, healthcare organisations and patient organisations, including tracking, reporting and annual disclosures. * Work with Legal and Ethics \& Compliance colleagues at global headquarters in Denmark to support the consistent application of global guidance across the UK site. * Explore appropriate uses of artificial intelligence to strengthen compliance monitoring and improve the efficiency of relevant processes and procedures. Who You’ll Work With You will report to the R\&D Quality, Ethics \& Compliance function within Novo Nordisk R\&D in Denmark but will be based out of Oxford site in UK. Your closest partners will include Novo Nordisk R\&D UK site colleagues and R\&D Legal. You will work across organisational boundaries, bringing together specialist perspectives and helping leaders move from regulatory complexity to clear, responsible action. What You Can Expect Here This is an opportunity to shape an Ethics \& Compliance programme with meaningful visibility and strategic scope. You will be trusted to apply your expertise and judgement, advise senior decision-makers and establish governance structures that support compliant R\&D delivery. You can expect close collaboration across the UK and Denmark, direct engagement with management and the opportunity to influence how compliance evolves in areas including data privacy and artificial intelligence. Application Support We are an equal opportunities employer, and we commit to an inclusive recruitment process and equality of opportunity for all our job applicants. If you're a person with a disability, if you're neurodivergent, and need any adjustments to be made during the application and selection process, please send an email to OHSY@novonordisk.com. Please include your name, the role you are interested in and the type of adjustment your need. Start now Your impact begins today. If you are ready to establish the governance, trusted partnerships and practical guidance that will strengthen Ethics \& Compliance across Novo Nordisk R\&D in the UK, apply for the Associate Director, R\&D Ethics \& Compliance role by 9 November We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. ,

Management Accountant (4316)

From $45,000/yr

Management Accountant (Part Qualified) – Kidlington – £45,000 Location: Kidlington, Oxfordshire Salary: £45,000 per annum Job Type: Permanent, Full Time Working Pattern: Office Based About the Client Our client is a growing international organisation with operations across multiple countries. They have established a strong reputation within their sector and offer a collaborative and supportive working environment. With a focus on continuous improvement and professional development, they provide employees with opportunities to broaden their experience and contribute to the ongoing success of the business. About the Job An excellent opportunity has arisen for a Part Qualified Management Accountant to join an established Finance team, reporting directly to the FP\&A Manager. This is a varied position offering exposure to management accounting, financial reporting, budgeting and business partnering. You will play an important role in maintaining financial controls, supporting operational decision making and contributing to the continued development of the Finance function. Duties will include: * Assisting with the preparation of monthly management accounts and ensuring reporting deadlines are achieved. * Preparing accruals, prepayments and balance sheet reconciliations. * Maintaining fixed asset records, including depreciation and asset movements. * Managing intercompany accounting and resolving reconciliation differences. * Reviewing overhead expenditure and investigating variances against budgets. * Producing financial analysis and cost centre reports for operational stakeholders. * Supporting monthly Group reporting, including submissions to the US parent organisation. * Assisting with budgeting, forecasting and financial planning activities. * Maintaining lease accounting schedules and supporting compliance requirements. * Providing financial information for internal and external audits. * Assisting with VAT, corporation tax and other statutory reporting obligations. * Identifying opportunities to strengthen financial controls and improve existing processes. About the Successful Applicant You will ideally be studying towards ACCA, CIMA or ACA, with previous experience in management accounting and month end reporting. Finalists and qualified by experience candidates will also be considered. Strong Excel skills, experience of balance sheet reconciliations and excellent attention to detail are essential. You will be confident communicating with stakeholders, managing deadlines and working within a busy Finance environment. What You Will Receive in Return You will receive a salary of £45,000 and the opportunity to join a growing international organisation offering exposure to both UK and US financial reporting. Working closely with an experienced FP\&A Manager, you will gain valuable experience across a broad range of accounting activities, with opportunities to develop your technical knowledge and commercial understanding. The organisation offers a supportive team environment, opportunities for professional development and the chance to make a meaningful contribution to business performance. This is an excellent opportunity for an ambitious Part Qualified Management Accountant looking to take the next step in their career.

Director, Clinical Trial Delivery

From $50/yr

Position Title: Director, Clinical Trial Delivery Department: N/A Reports to: CEO Compensation: Salary + equity options + benefits Company and role overview: Albus Health (www.albushealth.com) is a medical technology spin out company from the University of Oxford. We have developed Albus Home , a contactless multisensor platform that monitors sleep, vital signs and cough without the patients having to do, wear or charge anything. The product incorporates state of the art sensor technology, with sophisticated signal processing and AI/machine learning algorithms, collecting continuous, objective and accurate physiological data from the patient's home. Albus Home is available in over 50 countries, and has been used to collect over 10 billion data points across a dozen physiological and environmental parameters. Our clients include some of the world's largest pharmaceutical companies, and partners include some of the most reputed opinion leaders in medicine. Our team members have built unicorns in healthtech and biotech and are global leaders in medicine, drug development and healthcare technology. We are a lean and effective team, rapidly growing and actively recruiting across several functions. Albus Health is at an exciting stage at which we need to scale fast to meet the rapidly growing industry demand for our products and services. We are looking for a proactive and experienced Director of Clinical Trial Delivery to lead the delivery of Albus' solutions to world's top 10 pharmaceutical and CRO clients, ensuring the success of our clients in their clinical trials. This is a client-facing role that takes ownership of the entire delivery lifecycle and project management - setting up delivery strategies and processes, managing client relationships, overseeing logistics, tracking performance, and ensuring successful trial close-out. You will be the primary contact for clients throughout the lifecycle of the project and will work closely with internal teams across logistics and operations, technical support, regulatory and quality, and data delivery to continue timely, high-quality delivery of our product and services. This role has excellent growth and leadership opportunities, and will have significant influence on Albus' relationship with its clients. This is a critical hire as we scale our deployments globally across several continents, therapeutics areas and across phase I-IV clinical trials. Over time, you will be expected to build and manage the delivery team. You will need experience in global pharmaceutical clinical trials across the entire lifecycle, and understanding of deploying digital technologies or medical devices in global clinical trials, a strong understanding of the pharmaceutical clinical trials, and an operational mindset with high attention to detail. This is a full time position and reports to the CEO. Requirements Essential Duties and Responsibilities: Note: Other duties may be assigned. · Serve as the primary client-facing lead for delivery of Albus' technology in clinical trials, representing the company across delivery. · Own full delivery lifecycle — from protocol and contract review through project planning, ongoing project management, and closure. · Lead project management, including weekly client check-in meetings, tracking milestones, capturing risks and actions, managing escalations where necessary (both ways) and ensuring transparent progress reporting. · Improve, and where needed develop, SOPs for client delivery · Contribute to pre-sales discussions, providing strategic and operational input to proposals and partnership development. · Review Master Services Agreements (MSAs), Statements of Work (SOWs), and contracts to extract delivery obligations and translate them into clear operational plans and timelines, ensuring all internal and external stakeholders are coordinated. · Work with internal team members across operations, technical support, data delivery, business development, QARA and senior management · Coordinate with CRAs and sites (when needed) for materials preparation, training delivery, and ongoing operational support. · Ensure timely provision of regulatory and quality documentation, such as Instructions for Use, product specifications and regional regulatory certifications. · Manage study-specific data transfer agreements, confirming technical and legal alignment and coordinating secure data delivery to clients. · Ensure smooth trial closeout, including delivery of final data as per specifications, return of hardware, debriefs, and lessons learned. · Maintain detailed and traceable study documentation, ensuring compliance with internal SOPs and GCP. · Work cross-functionally with internal teams in operations, data, quality, product, and clinical to meet client expectations. · Drive continuous improvement in operational processes, documentation, and client satisfaction. Skills and Experience Essential: · 7+ years of experience with medical technology or services in clinical trials, preferably 3+ years with digital health technologies or within a small and rapidly growing team · 10+ years of experience in project management or client delivery roles · Demonstrated leadership of several multi-region end-to-end trial deployment in sponsor-facing roles · Advanced and operational understanding of clinical trial processes, pharmaceutical industry requirements and regulatory standards (GCP) and work knowledge of data and health standards (data protection, GDPR, HIPAA) · Demonstrated success managing multi-stakeholder client relationships. · Excellent organizational and project management skills, with attention to detail. · Strong written and verbal communication, especially for client and regulatory documentation. · Independent, resourceful, and proactive — comfortable owning projects end-to-end and working with varying degrees of seniority Desirable: · Experience delivering regulated devices or software in trials (e.g., Class I/II devices, CE/FDA, SaMD). · Understanding of data handling, security and compliance requirements (e.g., GDPR, HIPAA). · Familiarity with trial documentation platforms, eTMFs, or CTMS. · Experience in respiratory disease, digital biomarkers, or sleep monitoring domains. Benefits * Stock Option Plan * Pension Plan * Training \& Development * Cycle To Work Scheme * Exceptional growth opportunities in a rapidly growing startip

Data Analyst

From $45,000/yr

Data Analyst Up to £45,000 - Oxford Are you a Data Analyst who enjoys turning data into actionable insights and working closely with stakeholders to solve business challenges? We are working with an organisation that is continuing to invest in its data and analytics capability and is looking to add a BI Analyst to its growing team. This role will focus on delivering meaningful reporting, analysing business performance, and helping stakeholders make data-driven decisions through high-quality Power BI solutions. This is an excellent opportunity for someone who enjoys a blend of technical development and business engagement. You will work with a variety of stakeholders across the organisation, helping to understand reporting requirements, develop insights, and improve the overall use of data within the business. If you enjoy working with Power BI, writing complex SQL queries and translating data into clear business value, this could be a great next step in your career. Key Responsibilities * Developing and maintaining Power BI dashboards, reports and visualisations. * Gathering requirements from stakeholders and translating business needs into reporting solutions. * Writing and optimising SQL queries to extract, manipulate and analyse data. * Delivering insights and recommendations to support key business decisions. * Monitoring data quality and investigating reporting discrepancies. * Creating and maintaining documentation for reports, dashboards and KPI definitions. * Working closely with business teams to identify opportunities for improved reporting and analytics. Skills \& Experience * Strong SQL skills with experience querying and analysing large datasets. * Good commercial experience with Power BI, including dashboard development and data visualisation. * Ability to gather and understand business requirements from non-technical stakeholders. * Experience creating meaningful reports and presenting insights to the business. * Strong analytical and problem-solving skills. * Excellent communication and stakeholder management abilities. * Understanding of data modelling and reporting best practices would be advantageous. What's On Offer? * Up to £45,000 salary. * Hybrid working model (2 days per week in Oxford). * Opportunity to work closely with key business stakeholders. * Exposure to a variety of reporting and analytics projects. * Supportive team environment with opportunities for career progression. * Chance to make a tangible impact through data-driven decision making. * Whether you're an experienced BI Analyst or looking to build on your reporting and analytics expertise, this role offers the opportunity to work with modern BI tools while delivering real business value through data and insight.