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 Québec - Santé (FRQS).
Position summary
Department / Research Program: Gastroenterology
The incumbent is responsible for supporting the successful conduct of clinical research studies. The person will have to collaborate with investigators and health care teams to assume responsibility for the overall patient management and coordination of several clinical studies at the RI-MUHC.
General Duties
Under the direction of Dr. Amine Benmassaoud, the incumbent:
- Executes all aspects of study visits and collaborate with the entire medical care team.
- Performs clinical evaluation of the participants according to the protocol requirements,
- Recruits research participants:
- Maintains, completes and updates: adverse event log, questionnaires and protocol specific source documentation,
- Coordinates protocol related tests and processes and ships samples according to clinical protocol and manuals,
- Creates study specific source documentation,
- Provides coordination of all aspects of data collection and source documentation,
- Performs any other duties as assigned by the immediate supervisor.
Website of the organization
https://rimuhc.ca/en
Education / Experience
Education: Diploma of College Studies (DEC)
Work Experience: Two (2) years of related experience
Required Skills
- This position requires an advanced knowledge of oral and written French.
- An advanced knowledge of oral and written English is required, as the position requires regular and complex contact with patients who are exclusively proficient in English.
- Clinical research experience is an asset,
- Experience working with electronic data management systems, tools and technologies (EDC) is an asset,
- Experience working with Clinical Trial Management System (CTMS) is an asset,
- Knowledge of international, federal and provincial laws and regulations governing clinical research (ICHGCP) is an asset,
- Autonomous, flexible, sense of ethics and good judgment,
- Good organizational, time management skills, and ability to multi-task and prioritizing time-sensitive issues,
- Interpersonal skills.
Additional information
Status: Temporary Full-Time (35-hour workweek)
Pay Scale: Commensurate with education and experience
Work Shift: Variable
Work Site: GLEN Site, 1001 boul. Decarie
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If you wish to include a cover letter, please attach it with your resume in one document. ***
Why work with us?
- 6 days of paid sick leave per year, which includes a maximum of 3 personal day,
- Vacation calculated on a pro-rata basis based on a percentage of your salary,
- Modular group insurance plan (including gender affirmation coverage),
- RREGOP government pension plan (defined benefit plan),
- 5.3% of your gross earnings will be added to your paycheque in lieu of statutory holidays.
https://rimuhc.ca/careers
To learn more about our benefits, please visit http://rimuhc.ca/en/compensation-and-benefits
THIS IS NOT A HOSPITAL POSITION.
Equal Opportunity Employment Program
The Research Institute of the McGill University Health Centre hires on the basis of merit and is strongly committed to equity, diversity and inclusion within its community. We welcome applications from all qualified candidates who self-identify as members of racialized groups/visible minorities, women, Indigenous persons, persons with disabilities, ethnic minorities, and 2SLGBTQIA+ persons. We also welcome candidates with the skills and knowledge to productively engage with diverse communities. Persons with disabilities who anticipate needing accommodations for any part of the application process may confidentially contact, [email protected]
