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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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authorization for medical records as well as access to archived biospecimens and 2) sending requests for medical records and/or archival biospecimen acquisitions, • Data entry and management of online study
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best treatment strategies to improve clinical outcomes among patients with infectious diseases and other medical diagnoses. Areas of interest include but are not limited to bloodstream infections, C
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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