Summary
- Salary
- Competitive
- Team
- Science and Research
- Location
- 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, the Medical & Clinical Affairs function has been developed in the last years with a clear focus on innovation and research. 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 Trial Manager based in Singapore, working as part of the global Medical & Clinical Affairs team. This 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 be responsible for the successful trial management and coordination of clinical trials and human subject trials involving Dyson’s consumer healthcare products. This position focuses on overseeing various functions within the projects, ensuring seamless collaboration and effective execution. The Clinical Trial Manager will report to Clinical Affairs and work closely with cross-functional teams, internal stakeholders, vendors, and Contract Research Organizations (CROs) to ensure the trials are conducted in accordance with regulatory standards and company procedures. The role will involve:
Lead and manage trial projects, serving as the central point of contact for project-related activities. Ensure project goals, timelines, and objectives are clearly defined and met.
Collaborate with multidisciplinary teams, including design engineering, research, regulatory affairs and medical affairs, to align project strategies and ensure smooth communication across functions.
Develop comprehensive project plans, timelines, and budgets. Coordinate activities across functions to ensure the efficient execution of trials.
Contribute to the development of global capabilities and participate in the enhancement of processes within the Clinical Affairs department.
Oversee vendor and CRO activities, including contract negotiations, performance tracking, and deliverables management. Maintain strong relationships with external partners.
Contribute to trial design discussions, ensuring alignment with the internal stakeholders. Coordinate site selection, participant recruitment, data collection, and monitoring activities.
Maintain trial documentation, including essential files, regulatory documents, and investigator communications. Ensure documentation complies with Good Clinical Practice (GCP), regulatory requirements and company policies.
Collaborate with CROs to prepare essential documents and other necessary tools for the initiation of trial sites.
Identify potential risks and develop mitigation strategies to ensure trial success. Proactively address challenges that arise during the course of the project.
Collaborate with data management teams to ensure accurate and timely data collection, analysis, and reporting.
Provide regular updates on project progress, milestones, and challenges to relevant stakeholders and senior management.
Maintain familiarity with ICH-GCP, ISO 14155, other relevant regulations, company SOPs, and tracking systems. Ensure all activities are conducted in accordance with established standards.
Address project-related issues and deviations from plans promptly and effectively, working with teams to develop solutions.
Foster a collaborative and results-oriented team environment, providing guidance and mentorship to team members.
About you
University degree in Biology, Life Sciences, Biotechnology, or a related field.
At least 3 years of proven experience in project management applied to clinical research, preferably within the medical device industry.
Strong understanding of clinical trial processes, regulatory requirements, and industry best practices.
Excellent organizational skills, attention to detail, and proactive attitude.
Effective communication and interpersonal skills for seamless collaboration across functions.
Proficiency in ICH-GCP, other relevant regulations, and quality standards (ISO 14155).
Strong problem-solving abilities and adaptable to changing project requirements.
Ability to manage multiple projects simultaneously and prioritize tasks effectively.
Occasional international travel is involved.
Benefits
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.
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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.
