drjobs Clinical Research Coordinator - Nurse - Oncology (Research Institute)

Clinical Research Coordinator - Nurse - Oncology (Research Institute)

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1 Vacancy
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Job Location drjobs

Montreal - Canada

Monthly Salary drjobs

$ 43316 - 80425

Vacancy

1 Vacancy

Job Description

Do you want to work for a worldrenowned research institute that pushes the boundaries of biomedical science and health research Right here in Montreal! At the Research Institute of the McGill University Health Centre (RIMUHC) you can be part of an organization focused on scientific discovery and innovation in patientcentered medicine. Join us today and make a difference!

Job Description

RESEARCH INSTITUTE OF THE MUHC
The Research Institute of the McGill University Health Centre (RIMUHC) is a worldrenowned 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 RIMUHC is supported in part by the Fonds de recherche du Qubec Sant (FRQS).

Position summary
Under the supervision of the Manager of Oncology Research Centre for Innovative Medicine (CIM) the Clinical Research Coordinator Nurse is responsible for supporting the successful conduct of clinical research studies in oncology. The incumbent will collaborate with Investigators and health care personnel to assume responsibility for overall patient management and the coordination of several clinical studies for the CIMOncology Department of the RIMUHC.

The Centre for Innovative Medicine is located in the new Glen site hospital which is a unique center in Canada of 5000 m2 dedicated exclusively to clinical research.

More information on the CIM:
Duties
Obtains informed consent assesses patients for protocol eligibility through personal interviews and/or medical record review in inpatient and outpatient settings
Maintains and completes concomitant medication adverse events and questionnaires logs forms and protocol specific source documentation
Monitors patient safety and medication compliance
Prepares orders for protocol related requests and procedures consults prescriptions requests for pathology slides and blocks as needed
Coordinates all aspects of data collection and source documentation
Completes all research related documents and responds to queries and requests for information
Conducts protocol specific and scientific trainings
Creates protocol specific nursing alerts/feasibilities for the oncology day center
Responsible for assisting with the submission of serious adverse events to the Research Ethics Board
Conduct other related tasks as assigned by supervisor.

Website of the organization

video ( Si le poste est pour le CIM)


Required Experience:

IC

Employment Type

Full-Time

About Company

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