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biomedical sciences, bioinformatics, clinical research or related field strong clinical trial experience (design, execution, and regulatory submissions) proficiency in bioinformatics, statistical analysis (R
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ethical approval application, consent form and information sheet preparation, instrument development and validation, scale development, data cleaning and analysis, and report writing. Support the PI in
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Health or other related disciplines with at least 2 years of post-bachelor's work experience. Previous work experience in big data analysis, managing large databases of multiple research projects relating
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the analysis of large and complex datasets; iv) excellent written and oral communication skills; and v) the ability to work independently as well as in collaboration with a multidisciplinary team. Proficiency
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and validation, data analysis, report and manuscript writing, and public disseminations of findings. Support the PI in the coordination and monitoring of the instrument development and validation