drjobs Clinical Research Coordinator - MeDic Program (Research Institute)

Clinical Research Coordinator - MeDic Program (Research Institute)

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1 Vacancy
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Job Location drjobs

Montreal - Canada

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Job Description

RESEARCH INSTITUTE OF THE MUHC
The Research Institute of the McGill University Health Centre (RI-MUHC) is a world-renowned biomedical and hospital research centre. Located in Montreal Quebec the Institute is the research arm of the McGill University Health Centre (MUHC) affiliated with the Faculty of Medicine at McGill University. The RI-MUHC is supported in part by the Fonds de recherche du Qubec - Sant (FRQS).

Position summary
The Diabetes Modelling and Control group is looking for a recent (0 to 3 years) science graduate (physiology pharmacology immunology etc) for a clinical & regulatory research position. We lead a research program to develop automated insulin delivery systems (artificial pancreas) and to test new therapies (e.g. Ozempic) for people with type 1 diabetes.

The incumbent will have the opportunity to work with a multi-disciplinary team. Our team includes researchers with backgrounds of endocrinology engineering nursing pharmacology pediatrics and physiology. This is a great opportunity for a highly motivated applicant who wants to work on medical problems and learn about the clinical and engineering aspects of medical device and drug development.

General Duties
Write and design clinical trial protocols and participants consent forms
Recruitment of research participants train research participants on study protocol perform follow up calls and provide support over the phone
Complete study forms including case report forms and adverse events reports
Interact with research team (study physicians engineers and nurses) study funders and research ethics board
Support graduate students in their clinical research
Contribute to data analysis interpreting data presenting data and prepare visuals
Participate in the efforts for Health Canada submissions of Investigational Testing Authorization and Clinical Trial Authorization applications including writing all documentation.


Required Experience:

IC

Employment Type

Unclear

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