796 linked-data-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"https:" positions at University of British Columbia in canada
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-judgmental manner and present a range of solutions that will meet program and project goals and objectives. The incumbent develops research ethics submissions, data collection instruments and materials, data
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Summary The FMIS Business Analyst is responsible for the analysis, optimization, implementation, governance and ongoing enhancement of food management information systems supporting UBC Food Services
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, enhancing education and increasing physical activity levels and decreasing sedentary behaviour. - Builds and strengthens synergies between research, teaching and best practice, linking participation in
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information to applicants and/or their parents, many of whom are not familiar with the admissions process. The Admissions Coordinator also performs activities related to the control of documents and electronic
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providing complex information to applicants and/or their parents, many of whom are not familiar with the admissions process. The Admissions Coordinator also performs activities related to the control
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RNA medicines by linking molecular regulation of energy metabolism to functional outcomes in pre-clinical models. Candidate: The ideal candidate will hold a PhD in biophysics, biochemistry, molecular
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rewarding career. Job Summary The Research Assistant/Technician 2 supports data curation and specimen management activities across research studies within OVCARE and the AIM Lab, with a primary focus on the
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the general supervision of the Research Manager, the successful candidate will carry out a variety of assigned tasks supporting study start-up and ongoing implementation, including participant recruitment, data
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government partners and requires adherence to ethical, privacy, and data governance requirements. Emergency Departments (EDs) are critical low-barrier access points to the healthcare system and often the first
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. The Research Assistant will identify and screen potentially eligible participants, approach patients regarding study participation, obtain informed consent, and collecting and entering study data. A key