Job Description

Job Number:J0824-0790Job Title:Clinical Research Coordinator (Research Institute)Organisation:Research Institute of the MUHCWork Location:SITE GLENPosting Date:August 15, 2024Job Category:Research and teachingJob Type:Temporary full timeSalary:$43,316.00 - $80,425.80 /YearShift:DayOpen Positions:1RESEARCH 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 Qu\xc3\xa9bec - Sant\xc3\xa9 (FRQS).Position summary
We are recruiting a Clinical Research Coordinator to join the Pediatric Emergency Department at the Montreal Children\'s Hospital. Our emergency room cares for sick and injured children while conducting research projects to improve clinical outcomes and patient experience. Under the supervision of the Research Director, we are looking for a motivated, organized and enthusiastic person to join our dynamic team.ROLE:
More specifically, the clinical research coordinator will support initiation and coordination of a variety of projects with tasks including database management, entering data of all kinds (medical records, questionnaires, administrative data, laboratory data), controlling data entry quality, clinical follow-ups of research participants according to the study protocol, ensuring overall compliance with study protocols, and occasionally approaching families to participate in clinical research.
They will work collaboratively with the project leads, project manager, staff in the emergency department, community partners as well as patients & families.General Duties

• Conducts studies in the division of Pediatric Emergency Medicine, according to the protocols and guidance from the Director of Research of the Division (PEM-ADR),
• Works on several studies as needed, as discussed with the PEM-ADR,
• Submits studies to Research Ethics Board and ensures ethical approvals are continued throughout the study,
• Submits completed study manuscripts to scientific journals online platforms as required,
• Coordinates study initiation and ensures smooth and efficient day-to-day activities in the carrying out of the projects,
• Coordinates team meetings
• Monitors the progress of the research activities and prepares periodic and ad hoc reports,
• Completes regulatory documents and reports adverse events/amendment/deviation,
• Ensures compliance with protocol guidelines and requirements of regulatory agencies, if applicable,
• Coordinates study visits as per study protocol,
• Conducts patient prescreening based on patient medical charts,
• Recruits research participants as needed,
• Ensures proper documentation of investigator oversight,
• Conducts and/or verifies study questionnaires,
• Follows up with participants as per protocol,
• Performs data entry as required,
• Maintains adequate screening and enrollment records,
• Provides coordination of all aspects of data collection and source documentation, as per GCP guidelines and documents are completed in a timely manner,
• Communicates with investigators and other project stakeholders,
• Supervises and tracks Research Clerk activities,
• Collects clinical data, as well as patient information,
• Is implicated in the study budget and invoicing, as needed,
• Accomplishes any other relevant duties as required by the immediate superior and/or delegate.

Website of the organizationEducation / ExperienceEducation: Bachelor\'s Degree
Field of Study: Health-related fieldWork Experience: Minimum 3 years of recent clinical or administrative experience in a healthcare setting.Required Skills

• Excellent French and English, spoken and written (applicants will be screened for proficiency in both languages),
• Excellent communication and interpersonal skills,
• Ability to work independently or with teams with minimum supervision,
• Self-directed, organized and sense of ethics,
• Supervision experience an asset,
• Comfortable around children and in Emergency room setting,
• Experience in qualitative research and participatory research,
• Computer skills are necessary, Knowledge of Microsoft Office (Word, Excel, Power Point and Outlook).

Additional informationStatus: Temporary, full time (35 hours/week)
Pay Scale: 43,316.00- $80,425.80 Commensurate with education and experience
Work Shift: Monday to Friday 8:30am to 4:30pm
Work Site: GLEN Site, 1001 boul. DecarieWhy 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!

https://rimuhc.ca/careersTo learn more about our benefits, please visitTHIS IS NOT A HOSPITAL POSITION.Equal Opportunity Employment ProgramThe 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,

McGill University Health Centre