Clinical Research Job at RI-MUHC, Canada | Life Sciences | Earn $46.42 Per Hour | Apply Now
If you are an experienced clinical operations professional, a specialized oncology nurse, or a life sciences graduate loking to advance your career within advanced cellular therapeutics, this part-time opportunity at the Research Institute of the McGill University Health Centre (RI-MUHC) is an exceptional choice. Located on-site at the Glen Site in Montreal, Quebec, this position places you on the frontline of cutting-edge Chimeric Antigen Receptor T-cell (CAR-T) trials. For detail-oriented site operations specialists searching for a high-impact Clinical Research Job, this role offers hands-on mastery over leukapheresis scheduling, cell-processing lab coordination, and strict Health Canada compliance. It serves as an elite launchpad to expand a long-term Research Job portfolio and stands out as a premier selection for professionals tracking a competitive Life Sciences Job with a highly flexible, part-time schedule in a world-class academic hospital environment.
- Job Position: Clinical Research Coordinator
- Job Number: J0526-1018
- Work Location: SITE GLEN, Canada
- Job Category: Research and teaching
About the Institute
The Research Institute of the McGill University Health Centre (RI-MUHC) is a world-renowned biomedical and hospital research powerhouse. Operating as the research arm of the McGill University Health Centre (MUHC) and affiliated with the Faculty of Medicine at McGill University, the institute hosts over 1,200 researchers and spans complex clinical pipelines supported in part by the Fonds de recherche du Québec – Santé (FRQS). This specialized position is embedded within the Oncology (Phase 1, Complex Care) program at the Centre for Innovative Medicine (CIM). Working under the direct supervision of Program Manager Dr. Michael Sebag, you will join a highly integrated clinical team dedicated to bringing next-generation immuno-oncology treatments to life. Managing CAR-T trials here means bridging the gap between cell processing laboratories, blood product repositories like Héma-Québec, and inpatient units to deliver safe, patient-centered precision medicine.
Clinical Research Job – Key Responsibilities
The Clinical Research Coordinator (CRC) – CAR-T Therapy functions as the operational anchor for cellular therapy protocols, taking responsibility for interdepartmental scheduling, tracking databases, and strict regulatory maintenance.
Your core cellular logistics, data curation, and regulatory duties include:
- Cellular Therapy Lifecycle Coordination: Overseeing the critical logistics of CAR-T protocols, including scheduling patient procedures, leukapheresis timelines, lymphodepletion conditioning, CAR-T infusion windows, and long-term registry follow-ups.
- Standard Operating Procedure (SOP) Creation: Drafting and updating project-specific SOPs for complex cell therapies that integrate local clinical practice with cross-departmental hospital requirements.
- Multidisciplinary Stakeholder Liaison: Serving as the primary communications hub linking principal investigators, pharmaceutical sponsors, contract research organizations (CROs), Héma-Québec, and specialized processing labs.
- Regulatory Dossier Compliance: Preparing, tracking, and submitting essential regulatory documentation to ethics boards (REB), sponsors, and institutional systems (Nagano) in accordance with Health Canada Division 5 and GCP frameworks.
- Source Documentation & Auditing: Creating and maintaining accurate source files, answering data monitoring queries, and preparing the trial site for external audits and inspections to advance this Clinical Research Job.
- Clinical Unit Integration: Managing protocol-mandated workflows across the core hospital infrastructure, collaborating directly with oncology pharmacy teams, pathology rooms, and outpatient clinics to support a high-value Research Job.
- Site Staff Training Facilitation: Participating in and delivering protocol-specific site material training sessions, Site Initiation Visits (SIVs), and Clinical Trial Management System (CTMS) onboarding.
Qualifications & Profile Requirements For Clinical Research Job
The RI-MUHC seeks a highly organized, collaborative professional who possesses exceptional scheduling agility and can operate effectively in a fast-paced, highly regulated oncology environment.
- Required Academic & Experience Benchmarks:
- Educational Foundation: A completed formal Bachelor’s degree in Life Sciences or a closely related natural science/healthcare discipline to anchor a successful Life Sciences Job.
- Hospital Track Record: A minimum of 2 years of active experience working in a hospital or clinical research environment (with explicit preference given to oncology, hematology, or cellular therapy backgrounds).
- Core Linguistic & Technical Competencies:
- Mandatory Bilingualism: Professional working proficiency in French is required alongside an advanced knowledge of written and spoken English, as the role involves continuous complex contact with international researchers, multi-national sponsors, and diverse patient populations.
- Solid, practical understanding of clinical trial phases, Good Clinical Practice (GCP) guidelines, and Health Canada Division 5 regulatory standards.
- Strong digital workspace skills, including high proficiency in MS Office software and specialized research databases.
- Exceptional interpersonal communication and crisis-escalation skills to coordinate time-critical cell collection vectors smoothly.
Logistics, Shift Structures & Total Employee Rewards
- Location: Montreal, Quebec, Canada (Glen Site – 100% On-Site Workspace).
- Employment Status: Temporary, Part-Time Contract (15 hours per workweek).
- Work Schedule Framework: Day Shift (Exact hours to be arranged flexibly with the study doctors; occasional evening/overtime flexibility required based on patient cell infusion windows).
- Job Requisition Identifier: Job Number: J0526-1018.
- Hourly Wage Scale: $25.01 –
- $46.42 per hour
- (Starting compensation is commensurate with prior oncology research experience and academic qualifications).
- Financial & Sick Leave Benefits: 6 days of paid sick leave per year (including up to 3 personal days), pro-rated vacation allocations, and an additional 5.3% of gross earnings added to every paycheque in lieu of statutory holidays.
- Welfare Protection Plans: Access to a modular group insurance framework (including gender affirmation coverage) and the secure RREGOP government defined-benefit pension plan.
- Note: This position is hosted through the Research Institute (RI-MUHC) and is classified as a non-hospital payroll appointment.
In short, the Clinical Research Coordinator (CAR-T) position at the RI-MUHC is a definitive route to transitioning your oncology nursing or life sciences background into a premium asset at the forefront of immuno-oncology. Securing an appointment here allows you to bypass general entry-level data processing and take direct operational charge of the leukapheresis pipelines, cellular registries, and multidisciplinary logistics that bring life-saving gene therapies safely to clinical reality. If you reside in Montreal, meet the billingual requirements and the 2-year clinical baseline, apply today (attaching your cover letter and resume in a single document) to secure this premier selection in a Clinical Research Job, launch an exceptional Research Job, and lock in this outstanding Life Sciences Job.
