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). This position supports multiple key university graduate administrative services in FASS including: development of processes, application and admissions, student registration, records and progress tracking, degree
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accountability and alignment with CA2DM’s strategic objectives. Job Responsibilities Employment Research & Support - Assist in delivering high-quality employment support through: Conducting research to support
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University of Toronto | Downtown Toronto University of Toronto Harbord, Ontario | Canada | about 1 month ago
works with the Graduate Studies and Postdoctoral Affairs team to support programming for the UTM graduate and postdoctoral community. Your responsibilities will include: Tracking and monitoring
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: Assist with research for upcoming exhibitions, collection objects, and the museum's institutional history Support the development and implementation of exhibitions, including drafting object labels, wall
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status within the process. In this account, you are able to track your applicant status in "My Applications". To be considered eligible for the position as an internal candidate, departmental staff must
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medicine. The Institute is organised into six research centres which, though complementary and following the Institute’s strategic plan, also have Centre-specific objectives and requirements. The postholder
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and medicine. The key objective is to support efforts to advance biomedical research using computational methods. For more details, please view https://www.ntu.edu.sg/medicine/research/re search
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relate to ongoing research in the lab. Field Work: Assist with field-work as needed. Lab supplies: Assist in ordering; keeping track of supply inventory; unpacking lab supplies and putting them in proper
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investigador “César Nombela (2024-T1/BIO-31319) funded by "Comunidad de Madrid". Candidate profile: - Specialized researcher with an MSc related to plant biology and/or biochemistry. - Proven track record
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support: Assist with scheduling, user engagement, and tracking project activities Support recruitment and consenting of study participants under supervision Review clinical and patient records to support