Clinical Research Coordinator – Nurse - CIM - Phase 1 Oncology

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 Under the supervision of the Manager of Oncology Research, Centre for Innovative Medicine (CIM), the Clinical Research Coordinator - Nurse is responsible for supporting the successful conduct of clinical research studies in oncology. The incumbent will collaborate with Investigators and health care personnel to assume responsibility for the overall patient management and the coordination of several clinical studies for the CIM-Oncology Department of the RI-MUHC The Centre for Innovative Medicine is a hospital which is a unique center in Canada of 5000 m2 dedicated exclusively to clinical research. The CMI is located at the MUHC Glen site. General Duties Obtains informed consent, assesses patients for protocol eligibility through personal interviews and/or medical record review in in-patient and out-patient settings, Maintains and completes concomitant medication, adverse events and questionnaires logs, forms and protocol specific source documentation, Monitors patient safety and medication compliance, Prepares orders for protocol-related requests and procedures, consults, requests for pathology slides and blocks as needed, Coordinates all aspects of data collection and source documentation, Completes all research-related documents and responds to queries and requests for information, Conducts protocol specific and scientific trainings, Creates protocol specific nursing alerts/feasibilities for the oncology day center, Responsible for the Research Ethics Board submissions, Conduct other related tasks as assigned by the supervisor. Website of the organization https://rimuhc.ca/en Education / Experience Education: DEC in nursing is required. Bachelor's Degree is an asset. Experience: Minimum four (4) years of nursing experience including two (2) years in a hospital setting. Professional Membership: Good-standing member of the OIIQ Required Skills Advanced knowledge of oral and written French is required, An advanced knowledge of oral and written English is required, as the position requires regular and complex contact with patients, researchers or international students who are exclusively proficient in English, Solid written and verbal communication skills, Able to work under minimal supervision, Self-directed, flexible, organized and sense of ethics, Experience in hematology and/or oncology is preferred, Clinical research experience is an asset, Knowledge of international, federal and provincial laws and regulations governing clinical research (ICH-GCP) is an asset. Additional information Status : Temporary Full-time, maternity leave replacement. Pay Scale: Commensurate with education and experience. DEC Nurse: $45,518.20 - $84, 484.40 BAC Nurse: 57,093.40$ - 105,996.80$. Work Shift: 35 hours per workweek (flexible when needed day/evening/night, weekends on occasion). Work Site: Centre for Innovative Medecine, MUHC Glen Site. May have to travel on occasion. ***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! 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, research.talent@muhc.mcgill.ca

The coordinator is responsible for the overall patient management and coordination of clinical research studies in oncology. Key duties include obtaining informed consent, monitoring patient safety, and managing Research Ethics Board submissions.

A DEC in nursing and membership in the OIIQ are required, with a Bachelor's degree being an asset. Candidates must have at least four years of nursing experience, including two years in a hospital setting, and be proficient in both French and English.

• 4-week vacation • Personal and sick days • Paid statutory holidays • Modular group insurance plan • Gender affirmation coverage • Telemedicine • RREGOP government pension plan • Training and professional development • Child Care Centres • Corporate Discounts • Competitive parking rate • Employee Assistance Program • Recognition Program • Flex work options

• OrganizationPreferred

Identified from the job description. Confirm important requirements above.

• Patient Management
• Clinical Study Coordination
• Informed Consent
• Medical Record Review
• Data Collection
• Research Ethics Board Submissions
• French Proficiency
• English Proficiency
• Hematology
• Oncology
• ICH-GCP
• Nursing Care
• Communication Skills
• Organization

• Healthcare
• Science & Research

Minimum education

College diploma

Minimum experience

2+ years

Apply by

Sep 5, 2026

Posting language

English

Working hours

35 hours per week

Seniority

Mid-Senior level