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Clinical Research Scientist


Science and Research
Singapore - St James Power Station Headquarters

About us

Dyson is globally recognised as a pioneering and research-oriented engineering company. With a focus on consumer healthcare products within Dyson, a new Medical & Clinical Affairs function and team is being developed internationally with a clear focus on innovation and research.    

Medical Affairs serves as the scientific bridge between the industry and the wider medical community. This function is uniquely tasked with managing external relationships with key opinion leaders within the scientific community across a range of therapeutic specialisms, as well as with patient-consumer groups, authorities and beyond. 

Clinical Affairs are experts in clinical research and by integrating into an innovative engineering company, focus is on designing new methodologies and gathering essential evidence to drive new product category growth.  

We have a common vision of improving the quality of life of consumers through pioneering medical engineering in a safe and compliant way throughout the entire product lifecycle. 

About the role 

You will be a Clinical Research Scientist based in Singapore, working as part of the Global Medical & Clinical Affairs team.  

It is an incredible opportunity to take part in shaping the development of the future products at Dyson, pioneering scientific research and technology and enabling clinical evidence with exciting projects that drive real business value. 

You will have hands-on experience with all the technical and scientific aspects of clinical research leveraging expertise of a multi-disciplinary team and you will proactively contribute to the design, planning, execution and analysis of clinical trials in various therapeutic and consumer health’s areas.  

You will perform research intelligence and review available scientific data to develop solid product knowledge.  

You will develop study protocols including writing, reviewing and outlining the objectives and the methodology pertinent to each trial, as well as any other relevant documents required for the conduct of a clinical study.  

You will prepare and present protocols and reports as well as shape and define complex questions from the cross-functional teams and relevant stakeholders.  

You will engage with internal team members and external collaborators, including study investigators, contract research organisations (CROs), hospitals, research institutions, ethics committees and vendors. 

You will support Clinical Operations team to coordinate and review regulatory documents, Consent Forms (ICF), and other relevant trial materials.  

You will actively contribute to the ongoing review of clinical trial data to check safety procedures, efficiency and data accuracy and quality and you will facilitate the dissemination of the information on the trial progress among the relevant functions, i.e., the Global Medical & Clinical Affairs team, senior leadership team and external collaborators.  

You will provide inputs into the design of data capture systems, case report forms (CRFs) and the review and validation of clinical study reports (CSRs) with a thorough understanding of the connection between the collected data and the CSRs.  

You will team up with data managers, statisticians and other relevant project teams to perform the analysis and interpretation of the clinical data: you will verify data entered on to the CRFs are consistent with the source and support the development of first interpretable results, clinical investigation and evaluation reports, publications and internal/external presentations, including post-market follow-up studies. 

You will help build the global clinical capabilities by facilitating the identification, selection and management of the clinical sites/CROs.  

You will be involved in setting up trial sites, providing training to their staff and monitoring the trial throughout its duration from a medical/scientific/clinical perspective, which may require visiting the trial sites and compiling visit reports on a regular basis.  

Some travel may be required.  

Cutting edge approaches are key to keeping pace with Dyson’s innovative culture. You will be expected to stay abreast of industry trends and emerging technologies and methodologies. 

About you 

  • A Biomedical Science degree or other relevant degree or qualification. 

  • Minimum 3 years of experience in clinical research with proven experience of managing clinical investigations and evaluations from design, planning, obtaining ethics committee approvals, implementation and successful completion.  

  • Medical writing skills is essential. 

  • Excellent knowledge of the clinical trials in the Cosmetics, Medical Device, Pharmaceutical or CRO industry. 

  • Ability to work independently, creatively and with drive to make the clinical research team efficient and effective.  

  • Team player and good communication skills to be able to work closely with a range of skill sets within the project team. 

  • Knowledge and good understanding of the ICH GCP guidelines, industry-specific regulatory process and associated governance, including medical devices (i.e. ISO 14155: 2011 and IVD Directives).  


  • PhDs are valued, but innovation and excellence is essential. 

  • Statistical analysis skills are advantageous.  

  • Exposure and/or interest in emerging technologies with an application to clinical development, such as machine learning and digital health.   


Dyson Singapore monitors the market to ensure competitive salaries and bonuses. Beyond that, you’ll enjoy a transport allowance and comprehensive medical care and insurance. But financial benefits are just the start of a Dyson career. Professional growth, leadership development and new opportunities abound, driven by regular reviews and dynamic workshops. And with a vibrant culture, the latest devices and a relaxed dress code reflecting our engineering spirit, it’s an exciting team environment geared to fuelling and realising ambition.


Dyson is an equal opportunity employer. We know that great minds don’t think alike, and it takes all kinds of minds to make our technology so unique. We welcome applications from all backgrounds and employment decisions are made without regard to race, colour, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other any other dimension of diversity.

Interview guidance

We are following the government guidelines regarding COVID19. At this time all interviews will be conducted via video or telephone. We’re taking these precautionary measures to protect both our employee and candidate wellbeing. Our Talent Acquisition team will work with you and provide further information as appropriate.