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; Design, coordinate, and conduct semi-structured interviews and focus groups with key stakeholders (including Hospital Authority, Health Bureau, clinical experts, academics, and patient representatives
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, 3D simulation, preferably in orthopaedic- or medical-related projects. At least 3 years' experience in research coordination. Strong programming and data analysis skills with high implementation
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refinement Coordinate research projects, including ethics applications, data collection, and study logistics Administer questionnaires, manage research databases, and perform quantitative data analysis Conduct
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into the common data model. Conduct advanced statistical analyses and epidemiological studies on RWD. Collaborate with the Research Coordinators and Project Managers to define analysis plans and ensure data quality
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via scanning tunnelling microscopy maintain/refine the research instruments coordinate data collection and analysis assist in the preparation of reports and manuscripts perform other duties as assigned
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Responsibilities Assist the Principal Investigator in clinical research projects involving neurology patients with stroke or epilepsy Conduct literature review, coordinate projects, recruit subjects, prepare and
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to significantly reduce transport delays, improve material flow, and enhance coordination between logistics and manufacturing processes. c) Digital Twin System: We aim to construct a digital twin framework that
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with the Research Coordinators and Project Managers to define analysis plans and ensure data quality for specific projects. Prepare analysis datasets, reports, and visualisations for both internal
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, and presentations relevant to the project; Coordinate with internal and external stakeholders for the project; and Support other duties as assigned by the Principal Investigator. Requirements: A
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advanced therapeutics. Coordinate with clinical collaborators to obtain ethical approvals and obtaining human tissue samples for subsequent studies. Engage in collaborative projects both internally and