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Regulatory Affairs - Medical Devices (3 credits) Course overview: Biomedical Engineering : Regulatory strategies and quality management systems are critical for medical device development. This course provides
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for protocol eligibility through personalized interviews and/or medical record review in in-patient and out-patient settings, • Maintains and completes (either in paper or electronic formats) medication, adverse
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patients for protocol eligibility through personalized interviews and/or medical record review in in-patient and out-patient settings, • Maintains and completes (either in paper or electronic formats
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The Department of Biomedical Engineering of the Faculty of Medicine, McGill University, is seeking applications for a Course Lecturer for the 2024-2025 academic year to teach BMDE 558 Healthcare
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Education and Experience: DEC III - Medical Laboratory Technology 2 Years Related Experience / Hourly Salary: (MUNACA Level F) $29.42 - $36.46 Hours per Week: 35 (Full time) Supervisor: Lab & Purchasing
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that specimen samples collected for research purposes are transferred and stored in the appropriate facilities • Completion of case report forms (CRFs) from medical chart review, data extraction, evaluations, and
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studies. General Duties Working under the supervision of the clinic director, the incumbent will: • Supervise all aspects of the visits as part of the study and collaborate with the members of the medical
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medical terminology and academia (an asset); Excellent written and oral comprehension and communication skills in French; Autonomy in the execution of its mandates; Good ability to set priorities and
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at McGill University), do not apply through this Career Site. Login to your McGill Workday account and apply to this posting using the Find Jobs report (type Find Jobs in the search bar). Faculty of Science
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of l’Ordre professionnel de la physiotherapie du Quebec . Work in close collaboration with the interdisciplinary medical group of the clinic. Participate in mentorship sessions as required. Provide sport