749 programming-"Multiple"-"Prof"-"Humboldt-Stiftung-Foundation"-"O.P"-"U"-"U.S" positions in Canada
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across multiple units. Central VPRI resources includes Executive Leadership, Communications, Human Resources, Institutional Chair Programs, and Strategic Initiatives. The role also includes any ad-hoc
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day to day direction from the SP Coordinator and the Administrative Coordinators. This position will assist with the promotion, development, and coordination of the Simulated Patient Program (SPP
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progress. Supervision Given May provide guidance to student assistants and/or support staff on research or project teams. Minimum Qualifications Completion of a relevant technical program or a university
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an asset. 5 - 8 years of professional experience coordinating programs and projects involving multiple stakeholders and competing deadlines. Thorough understanding of the post-secondary environment and
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practices. Qualifications: A PhD in the Social Sciences or the Humanities. Strong research and writing skills, demonstrated in the publication of multiple peer reviewed journal articles. Deep familiarity with
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requires a high degree of independence, initiative, and problem-solving ability to manage multiple priorities and respond to evolving program needs. Reporting to the SRS Programs Manager, the MPT Program
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on behalf of the Division, requiring knowledge in all live education programs across multiple portfolios. Generates complex financial and registration reports. Responsible for the custom registration portals
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requires a high degree of independence, initiative, and problem-solving ability to manage multiple priorities and respond to evolving program needs. Reporting to the SRS Programs Manager, the MPT Program
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: Creative Destruction Lab (“CDL”), originated at the Universityof Toronto’s Rotman School of Management, is one of the world’s premier seed stage programs for massively scalable science-based ventures
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the supervision of the Clinical Research Unit Manager, the incumbent will perform the following duties: Primary Responsibilities: 1. Administer clinical trial screening activities across multiple sites (e.g