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 differenceJob DescriptionRESEARCH INSTITUTE OF THE MUHCThe 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 SummaryThe 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 DutiesParticipant Screening and RecruitmentConduct 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.Informed Consent ProcessClearly 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.Coordination of Study VisitsSchedule (including booking, confirming and rescheduling appointments), conduct, and document study visits in a timely fashion and as outlined in the protocol.Data and Sample CollectionCollect clinical and survey data as well as biospecimens from the participants,Accurately enter data into electronic data capture systems (REDCap) and maintain source documents.Participant Engagement and RetentionMaintain communication with participants for visit reminders, health status updates, and support participants in alignment with study procedures and protocol.Documentation and Regulatory ComplianceEnsure 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.Interdisciplinary CoordinationCollaborate with investigators, trial nurses, lab personnel, trial manager,



and research coordinators,Attend study meetings and contribute to team communications and updates.Quality Assurance and Monitoring SupportSupport 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.Training and Onboarding SupportParticipate in study initiation meetings and protocol/study procedures' training,Support the onboarding of recent site staff by sharing workflows, SOPs, and protocols.Website of the organizationEducation / ExperienceEducation: Diploma of College Studies (DEC)Field of Study: DEC in Nursing or BScN/BNI in Nursing.Good Clinical Practice (GCP)Work Experience: 2-3 yearsProfessional Membership: YesNurse Clinician or registered nurse in good standing with OIIQ certification.Required SkillsExcellent 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 informationStatus: Temporary, full time (35-hour workweek)Pay Scale: $44, $103, Commensurate with education and experienceWork Shift: Monday to Friday 8:00am to 4:00pmWork 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,

📌 Nurse (Full-Time) - C$44 - C$103 An Hour (Montreal)
🏢 McGill University Health Centre
📍 Montreal