Job Title

About TidalSense: TidalSense is a respiratory technology company with a mission to transform the diagnosis, monitoring and management of chronic respiratory conditions, such as asthma and COPD. The company has ambitions to enable a population-scale change in respiratory care through global deployment of its technologies in both developed and developing countries with poor access to healthcare. TidalSense has launched the first-of-its-kind AI-driven (software medical device) diagnostic test for COPD which uses the companys unique, patented, sensor technology embedded in the N-Tidal Handset medical device. We are seeking a motivated clinician with strong research and scientific writing skills. We are at an exciting phase in our journey as we transition from a start-up to a scale-up. You will be joining a passionate, socially-motivated and multi-disciplinary team covering engineers, scientists, clinicians, designers, product and usability specialists. This is a unique opportunity for a driven and autonomous individual to generate the clinical evidence and insights that will drive development, regulation, and commercialisation of our medical devices, delivering impact in the real world and changing peoples lives. We are seeking someone who is comfortable working in a fast-paced, agile, and diverse team environment, and who is also committed to our mission to revolutionise respiratory medicine. Job purpose: To take a leading role in the generation of clinical evidence and scientific content to support the regulation, scientific profile, and adoption of TidalSenses medical devices. Key duties & responsibilities: Clinical research Provide input to the design and develop of clinical research programmes including regulatory validation studies, exploratory research studies and real-world evidence studies. Write project charters, study protocols, ethics submissions and other required study documentation, and support ongoing study management. Lead clinical data gap analyses to identify where further evidence is needed for product / feature development, new market access, reimbursement, or clinical adoption. Critically analyse current clinical processes, and design / implement process improvements to optimise efficiency and delivery of targets. Scientific writing Write, review and edit clinical scientific content, including: peer-reviewed scientific publications, conference abstracts, white papers, scientific and clinical marketing content, product manuals and educational materials. Support with writing grant applications for (clinical) research programmes. Stakeholder management Work closely with the clinical, commercial and marketing teams to support key clinical stakeholder management, including building and maintaining a network of key opinion leaders to support current and future studies. Regulatory Plan, run and report systematic literature searches / reviews to support regulatory submissions. Skills & Competencies Essential: Excellent written and verbal communication skills, with the ability to describe complex scientific concepts for diverse audiences. Strong analytical and research skills, including the ability to conduct systematic literature searches, design studies, and interpret data. Strong organisational and project management skills (no formal qualification required). Ability to deliver to deadlines, comfortable with uneven workloads. Attention to detail. Ability to work autonomously. Willingness to learn and develop processes and personal skills. Views Generative AI and automation tools as a ''force multiplier'' for their own productivity and is eager to pioneer new workflows in a regulated healthcare environment. Desirable: Knowledge of clinical study / trial methodologies, including endpoint selection, bias mitigation, and statistical power / sample size calculations. Health economic modelling Qualifications & Experience Essential: Qualified healthcare professional (e.g. doctor, nurse or other allied health professional). Experience in clinical scientific writing, including publication of articles in peer-reviewed journals. Experience of designing, managing or delivering clinical research projects. Experience of project management. Desirable: Masters, PhD or DPhil in a scientific or clinical subject. Experience of protocol / bid / grant writing. Experience working with medical device products in an industry role. Other Requirements This role requires existing unsponsored UK right to work. Please note we cannot sponsor initial entry into the UK. We are, however, able to offer sponsorship for visa extensions or switches for current employees following a successful probationary period. Will need to be able to work in person in the Cambridge office at least 3 days / week (but ideally more). Salary 45,000-75,000 (depending on experience) TidalSense operates a fair pay structure to ensure our colleagues are paid equitably and competitively for their skill, expertise and experience. Successful candidates will be offered this role at the appropriate grade, based on both their resume experience and our judgement of their performance level through the assessment process. Flexible working hours to support your work preferences Hybrid working as per requirements above 25 days annual leave + 8 public holidays Pension: TidalSense contributes 5% of qualified earnings (increasing to 6% of base pay from H2 2026) Private health insurance (from H2 2026) Annual performance-based bonus Discretionary share options scheme Work from abroad for 1 week per year Buy / sell up to 5 days annual leave (pro-rated) Individual personal development budget + dedicated development days Mental Health support: wellbeing support and free 24/7 access to qualified counsellors and advisors Coaching and mentoring Team events and celebrations Beautiful award-winning Cambridge UK office stocked with quality drinks & snacks #J-18808-Ljbffr