Healthcare jobs in Oxford

What you would do

• Develop and execute the global IP strategy aligned with R&D and business objectives.
• Manage the patent and trademark portfolio, including prosecution timelines, renewals and jurisdictional requirements.
• Draft and file new patent applications in partnership with external IP counsel.
• Assess novelty and inventiveness of invention disclosures and prioritise ideas for protection.
• Provide freedom-to-operate guidance to R&D and escalate material IP risks.
• Support responses to IP challenges and disputes in coordination with external counsel.

Skills

What you would do

• Develop systems to evaluate and improve evidence capture for outstanding care service.
• Maintain robust monitoring, evaluation, and quality assurance systems, reporting concerns to the Registered Manager and Director.
• Support teams to deliver results meeting client and governing body expectations.
• Ensure outstanding compliance to achieve positive feedback from CQC, Local Authority, and Right at Home inspections.
• Plan, allocate, and evaluate quality of work and training needs for staff.
• Ensure consistent application of Right at Home policies, procedures, and approved practices.

Skills

What you would do

• Receive, log, process and track clinical and laboratory samples, maintaining accurate sample identification and traceability.
• Perform microbiology workflows including culture preparation, plating, colony counting, culture enumeration and preparation of isolates for downstream applications.
• Perform molecular biology workflows including nucleic acid extraction, quantification and sample preparation for downstream analysis.
• Perform routine sample and assay quality control, including microbiological and molecular QC.
• Perform qPCR assays and support interpretation and documentation of QC results.
• Prepare samples and libraries for sequencing.

Skills

What you would do

• Lead daily Patient Access team operations and drive team performance accountability.
• Monitor and drive Patient Access metrics (callbacks, bedside, NPS, RQA).
• Verify patient benefits, check patients in and out, and collect copayments, coinsurance, and deductibles.
• Create and maintain the Patient Access schedule for the assigned location and cover voids or coverage gaps.
• Train and mentor new Patient Access staff, assist with candidate interviews, and complete first 90-day reviews.
• Implement Patient Access policies and procedures with leadership input.

Skills

What you would do

• Design and execute molecular validation experiments using established protocols.
• Perform molecular biology workflows including DNA/RNA extraction and QC, reverse transcription, PCR/RT-qPCR, cloning and construct handling.
• Handle and process human tissue samples for RNA/DNA extraction and HLA typing per HTA regulations.
• Conduct cell- and tissue-based assays including transient transfections and FACS.
• Analyse and interpret experimental data and recommend next steps.
• Troubleshoot technical issues and improve assay quality and reproducibility.

Skills

What you would do

• Own the end-to-end UAT process for IT deliverables across project and BAU release cycles.
• Develop and maintain UAT strategies, plans, schedules, and test approaches aligned to delivery timelines.
• Define UAT entry and exit criteria and ensure testing readiness before execution.
• Coordinate UAT activities across multiple concurrent releases and initiatives.
• Manage testing risks, dependencies, assumptions, and issues through to resolution.
• Ensure appropriate business representation and stakeholder participation throughout testing activities.

Skills

What you would do

• Providing routine hygiene and periodontal treatment to an established patient base.
• Delivering 30-minute routine hygiene appointments and 60-minute periodontal treatment appointments.
• Seeing Direct Access patients.
• Working independently within a supportive dental team.
• Performing decontamination procedures on-site.

Skills

What you would do

• Translate validated functional and phenotypic assays into automation-ready protocols.
• Design, adapt, optimize and validate automated workflows for cell-based screening assays.
• Partner with automation engineers to troubleshoot and improve automated protocols.
• Execute medium-throughput functional genomics and phenotypic screening campaigns.
• Analyze assay performance and screening datasets to monitor platform performance and drive continuous improvement.
• Implement new automation technologies, digital tools and data-enabled solutions.

Skills

What you would do

• Develop, post, and maintain job advertisements and recruitment materials tailored to target audiences and sourcing channels.
• Proactively source and engage qualified candidates via LinkedIn, job boards, networking, talent pools, and referral programs.
• Conduct candidate screening, first-round interviews, assessments, and provide interview feedback to hiring managers.
• Maintain the Applicant Tracking System with candidates, requisitions, and recruitment activity records.
• Build candidate pipelines for open and future opportunities.
• Partner with hiring managers to understand business and recruitment needs.

Skills

What you would do

• Lead pilot projects demonstrating Oxford Nanopore's utility in priority markets and strategic application areas, working with internal and external stakeholders and customers.
• Provide technical guidance, VOC and feedback to product development teams on performance and strategy.
• Coordinate and deliver all sequencing and analysis including sample transfer, sample processing, data QC, data management, raw results, visualization and interpretation.
• Maintain documentation of data, analysis, and customer reports using best practices for reproducible research.
• Manage cross-functional communication, projects, and deliverables with internal and external teams.
• Work closely with commercial teams and key accounts on pilot projects to deliver scientific data leading to sales.

Skills

What you would do

• Conduct and report onsite monitoring visits.
• Perform CRF review, source document verification and query resolution.
• Manage site communication and relationships with clinical sites and investigators.
• Act as point of contact for in-house support services and vendors.
• Communicate with internal project teams on study progress.
• Participate in feasibility research.

Skills

What you would do

• Work embedded within DMPK research teams on disease programs.
• Perform DMPK in-vitro assays and apply them to prediction of pharmacokinetics.
• Conduct drug metabolism and enzymology experiments.
• Support assay development and optimization.
• Gain hands-on experience of the drug discovery process in a multidisciplinary laboratory team.

Skills

What you would do

• Characterising and modifying surfaces and interfaces to improve sensor chip technology.
• Researching and developing novel membrane formulations.
• Supporting electrophysiology-based experiments.
• Designing experiments, analysing data, and communicating findings to stakeholders.
• Collaborating across R&D teams to advance platform chemistry and support IP generation.
• Transferring processes and documentation to wider teams.

Skills

What you would do

• Perform egg collections.
• Manage embryo transfer lists.
• Conduct fertility consultations.
• Carry out HyCoSy and saline procedures.
• Perform SSR procedures where desirable.
• Collaborate with medical, nursing and other colleagues within a multi-disciplinary fertility team.

Skills

What you would do

• Providing personalised end-of-life care to people in their own homes as part of a community team.
• Supporting individual care plans by assisting with personal care, skin integrity, nutrition and hydration, mobility, rest and sleep.
• Maintaining a clean and safe care environment.
• Observing and responding to changes in a person's condition and supporting symptom management within the agreed care plan.
• Escalating concerns promptly to registered healthcare professionals.
• Communicating calmly and sensitively with patients and loved ones, preserving dignity, choice and wellbeing.

Skills

What you would do

• Own the lab systems end to end: lab information system, scanners, automations, servers, network and cloud platform integrations.
• Own the release cycle: impact assessment, testing, validation, rollback planning and go/no-go decisions.
• Lead service recovery: restore service and fix root cause.
• Manage lab software suppliers, agree priorities and hold them to agreed dates.
• Plan downtime and change windows with the lab.
• Implement monitoring, disaster recovery and business continuity.

Skills

What you would do

• Perform contamination testing including mycoplasma testing.
• Operate autoclave systems and manage waste streams.
• Coordinate steri-cycle runs and BSC decontamination schedules.
• Oversee monthly lab cleanings and change sticky mats.
• Schedule and manage deliveries of lab supplies and equipment.
• Oversee truck staging at loading docks.

Skills

What you would do

• Dealing with high volumes of patient notes; preparing clinics and administration duties involved with medical records; supporting the transaction of the medical records process; preparing clinical notes for outpatient and inpatient departments; working calmly in a high volume department.

Skills

What you would do

• Prepare amplified template libraries for high-throughput sequencing.
• Carry out DNA sequencing on next-generation DNA analyzers.
• Perform routine maintenance of DNA analyzers and related equipment.
• Check inventory and replenish consumable sequencing supplies.
• Communicate with customers by phone and e-mail.
• Follow SOPs and guidance of supervisors.

Skills

What you would do

• Exchanges data, documents and project information between investigative sites, site vendors and the project team.
• Ensures order, receipt, inventory storage, distribution, return/recall and reconciliation of clinical supplies.
• Handles administrative financial tasks.
• Coordinates preparation for and follow-up on site, TMF and systems audits and inspections.
• Maintains study-specific and corporate tracking systems.
• Maintains Trial Master File (TMF) and performs TMF review and oversight at country and site level.

Skills