
TidalSense is a venture-backed respiratory technology company founded in 2013, headquartered in Cambridge, UK. The company is dedicated to revolutionizing respiratory care through AI-driven…

TidalSense is a venture-backed respiratory technology company founded in 2013, headquartered in Cambridge, UK. The company is dedicated to revolutionizing respiratory care through AI-driven…
Founded: 2013
Headquarters: Cambridge, UK
Product: N-Tidal (Diagnose & Capture) — CE-marked Class 2a device for COPD diagnosis
Tech: Patented CO2 sensor + AI cloud platform
Recent funding: Seed round May 2023 (~£7.5M) led by BGF & Downing Ventures
Respiratory diagnostics and remote patient monitoring for obstructive lung disease (e.g., COPD, asthma).
2013
Software Development
£7.5 million
Reported May 16, 2023 round; company cites ~£13M in financial support to date from investors and funders including BGF, Downing, Foresight Group, Innovate UK, SBRI Healthcare, NIHR and Asthma + Lung UK.
“Backed by institutional investors including Business Growth Fund (BGF), Downing Ventures and Foresight Group; has received grant and public fund support (e.g., Innovate UK, SBRI Healthcare, NIHR).”
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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 company's unique, patented, sensor technology embedded in the N-Tidal Handset medical device.
We are seeking a clinical scientist with strong research, scientific writing, and project management 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 people's 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 TidalSense's medical devices.
Key Duties & Responsibilities Clinical research
Contribute to the creation and development of the company's global clinical evidence strategy
Scientific writing
Stakeholder management
Clinical evaluation and regulatory
With support from the rest of the clinical team, take a leading role in the planning and execution of clinical evaluation in accordance with EU MDR and other applicable regulatory requirements for existing and new medical devices, including:
Writing and reviewing Clinical Evaluation Plans and Reports and Post-Market Clinical Follow-up Plans and Reports
Planning, running and reporting systematic literature searches
Requirements Skills & Competencies Essential:
Qualifications & Experience Essential:
Desirable:
Other Requirements
Note to Applicants
Closing date for applications: Sunday 22nd February 2026
Benefits Salary £40,000-75,000 (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.
We are open to interviewing more junior candidates as well as those who have more industry experience in role.
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Design, plan and project manage research programmes
Write project charters, study protocols and ethics submissions and other required study documentation
Contribute to and oversee study implementation, monitoring and close out, including:
site visits;
formal study reporting and registrations; and
communications with external stakeholders (eg MHRA, grant monitoring officers)
Critically analyse current clinical processes, and design / implement process improvements to optimise efficiency and delivery of targets