drjobs Clinical Research Coordinator, Phase 1 (Research Institute)

Clinical Research Coordinator, Phase 1 (Research Institute)

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1 Vacancy
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Job Location drjobs

Montreal - Canada

Monthly Salary drjobs

$ 44408 - 82427

Vacancy

1 Vacancy

Job Description

Do you want to work for a world-renowned 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 (RI-MUHC) you can be part of an organization focused on scientific discovery and innovation in patient-centered medicine. Join us today and make a difference!

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
Under the supervision of the Manager of Phase 1 Research at the Centre for Innovative Medicine (CIM) the Clinical Research Coordinator is responsible for supporting the successful conduct of clinical research studies. The person will collaborate with Investigators and health care personnel to assume responsibility for the overall patient management and coordination of several clinical studies for the RI-MUHC.

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

More information on the CIM:
Duties
Recruits research participants prescreens patients and obtains informed consent assesses 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) medication adverse events and questionnaires logs forms and protocol specific source documentation ensures ethical approvals are continued throughout the study
Monitors patient safety and medication compliance
Completes all follow-ups as per special protocol requirements: patient visits/status disease site active trial lists and completes clinical notes
Coordinates orders for protocol related requests and procedures: consultations requests for pathology diagnostic and analytical laboratories etc
Coordinates all aspects of data collection and source documentation
Completes all research related documents and responds to queries and requests for information
Collaborates and acts as a liaison with the various departments within the Research Institute and the MUHC as well external parties
Conduct other related tasks as assigned by the Supervisor/Manager.

Additional information

Status : Temporary Full-Time (35-hour workweek)
Pay Scale: Commensurate with education and experience. $44408.00 - $82427.80.
Work Shift: Monday to Friday 8:30am to 4:30pm. Occasionally evening & night shift.
Work Site: GLEN Site 1001 boul. Decarie

***If you wish to include a cover letter please attach it with your resume in one document. ***

Why work with us

4-week vacation 5th week after 5 years
Bank of 12 paid days (personal days and days for sickness or family obligations)
13 paid statutory holidays
Modular group insurance plan (including gender affirmation coverage)
Telemedicine
RREGOP (defined benefit government pension plan)
Training and professional development opportunities
Child Care Centres
Corporate Discounts (OPUS Perkopolis)
Competitive monthly parking rate
Employee Assistance Program
Recognition Program
Flex work options and much more!


learn more about our benefits please visit
IS NOT A HOSPITAL POSITION.


Required Experience:

IC

Employment Type

Full-Time

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