Your Opportunity:
Alberta Health Services (AHS) continues to garner recognition as one of the best places to work in Canada and has made the list for Alberta\'s Top 75 Employers and Canada\'s Best Diversity Employers. Our employee benefits, culture and work-life balance are some of the many reasons we are an employer of choice. The University of Alberta Hospital (UAH) is one of Canada\'s leading academic health sciences centres with a reputation for clinical research, innovation, education, and patient-centred care. The University of Alberta Hospital (UAH) is one of Canada\'s leading academic health sciences centres with a reputation for clinical research, innovation, education, and patient-centred care. The Clinical Trials Unit supports the Principal Investigators in conducting research studies at AHS/UofA and within the Edmonton zone. Embedding research, innovation and analytic capacity in the healthcare system helps ensure AHS provides patient-focused, quality healthcare to more than four million Albertans. The Clinical Trials Unit is recruiting for a Research Coordinator to provide support for clinical research trials. You will be assigned to the Cardiology group at the Mazankowski Heart Institute. The Mazankowski Heart Institute is a world leader in complex and cardiac care.The main responsibilities of this position includes the identification and consenting of eligible participants collection and documentation of clinical trial data. This position will require exceptional organizational skills that are necessary to manage multiple trials and ensure that study information is timely, accurate, valid according to the study protocol, sponsor and Health Canada Regulations, when applicable. Working under limited supervision, you will perform diversified duties requiring independent judgement and confidentiality.
Description:
As a Research I, you will be working with research teams which are generating and disseminating new knowledge that assists with advancing the understanding of health disciplines and various health and medical concerns. Working under the guidance of the principal investigator, you will be responsible for preparing and submitting research documents, collecting and reviewing a variety of information related to the study, and monitoring study compliance. You will also assist with the recruitment of study participants and initiate consenting of study and/or trial participants and may complete lab work to support research activities.
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