Nurse (full-time)

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 Québec - Santé (FRQS).

Position summary
The Personalized Transplant Care Research Program seeks to inform on strategies to improve outcomes and experiences of people living with immunocompromising conditions.
The incumbent will be responsible for participant recruitment as well as conduct of trial activities including but not limited to participant recruitment vaccine administration data and sample collection clinical follow-up and documentation at the site level. This includes ensuring compliance with the study protocol institutional policies and regulatory guidelines. The incumbent will work under the supervision of the Principal Investigator and in consultation with the.

This position plays a vital role in ensuring participant safety enhancing engagement and maintaining the integrity and quality of study procedures.

General Duties
Screening and Recruitment
Conduct pre-screening assessments in alignment with inclusion/exclusion criteria
Perform eligibility assessments in accordance with protocol-defined inclusion/exclusion criteria
Coordinate and schedule informed consent discussions with eligible participants.

Consent Process
Clearly explain study objectives procedures and risks/benefits to potential participants in alignment with the trial protocol
Obtain and document informed consent in compliance with ethical and regulatory standards.

of Study Visits
Schedule (including booking confirming and rescheduling appointments) conduct and document study visits in a timely fashion and as outlined in the protocol.

and Sample Collection
Collect clinical and survey data as well as biospecimens from the participants
Accurately enter data into electronic data capture systems (REDCap) and maintain source documents.

Engagement and Retention
Maintain communication with participants for visit reminders health status updates and support participants in alignment with study procedures and protocol.

and Regulatory Compliance
Ensure compliance with ICH-GCP and institutional policies
Document adverse events and protocol deviations and report them in accordance with Sponsor Regulatory Authorities (e.g. Health Canada) RI-MUHC SOPs and REB guidelines.

Coordination
Collaborate with investigators trial nurses lab personnel trial manager and research coordinators
Attend study meetings and contribute to team communications and updates.

Assurance and Monitoring Support
Support audit and monitoring visit preparation by ensuring documentation is complete and up to date
Respond to queries from monitors auditors and study supervisors and implement corrective actions if needed.

and Onboarding Support
Participate in study initiation meetings and protocol/study procedures training
Support the onboarding of new site staff by sharing workflows SOPs and protocols.

Website of the organization

/ Experience

Education: Diploma of College Studies (DEC)
Field of Study: DEC in Nursing or BScN/BNI in Nursing.
Good Clinical Practice (GCP)

Work Experience: 2-3 years

Professional Membership: Yes
Nurse Clinician or registered nurse in good standing with OIIQ certification.

Required Skills

Excellent command of French and English both spoken and written.
Strong verbal and written communication skills demonstrated ability to interact professionally with participants colleagues and multidisciplinary teams.
Ability to work independently and exercise sound judgment with minimal supervision.
High level of accuracy in documentation data entry and protocol adherence.
Working knowledge of clinical and research software systems including REDCap Medvisit and OACIS.
This position requires onsite presence.
Adaptability to evolving demands.
Patient-centred approach.

Additional information

Status: Temporary full time (35-hour workweek)
Pay Scale: $44408.00- $103412.40. Commensurate with education and experience
Work Shift: Monday to Friday 8:00am to 4:00pm
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.

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