23 data "https:" "https:" "https:" "https:" "Uppsala universitet" Postgraduate research jobs at University of British Columbia
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Staff - Non Union Job Category Non Union Technicians and Research Assistants Job Profile Non Union Hourly - Research Assistant /Technician 2 Job Title CLSA Data Collection Site- Research Assistant 2
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and Associate Dean, Research. This position provides authoritative information to a variety of stakeholders on grant application opportunities and processes and entails detailed knowledge of granting
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governing the activities of the institution. Any procedures or data recorded must be accurate and must accurately reflect the work performed. Strict confidentiality of all study participants must be adhered
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with graduate students, principle investigators and farm staff. Work Performed Supports the AHWR Manager in collecting routine animal health data [e.g., body condition score (BCS), subclinical ketosis
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. The incumbent will support the operational and data-related functions of cardiology and heart failure research projects led by Dr. Nathaniel Hawkins, and will interact predominantly with the Research Project
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databases, entering data according to established protocols. Cleans and performs basic maintenance of equipment and apparatus. Carries out any other related duties as required . Consequence of Error/Judgement
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overseeing daily operations and finances of the youth mental health lab. This position will also lead group analysis of data, assists in preparation of grants, ethics application, summary reports and
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of data, assists in preparation of grants, ethics application, summary reports and publications. WORK PERFORMED: Works in co-operation with members of the research team and following research ethical
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maintaining daily care of laboratory mice; changing and cleaning animal cages, and racks; maintaining mouse data; disinfecting rooms; and general upkeep of the animal facility in accordance with unit Standard
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to the coordination of research activities, including obtaining and documenting informed consent, arranging sample collection and shipping, consolidation of clinical patient data, participating in case discussions and