Education LevelMaster's degree in a relevant field of studyCareer LevelRequires 6 years of relevant experience, including 1 year of supervisionHourly RateGrade 11: $41.99 - $59.09 (hourly)LocationJuravinski Hospital, TRACE Unit, Research Centre, G Wing, 1 st FloorEmployee GroupUNIFOR Local 5555, Unit 1 Bargaining UnitJob TypeContinuing, subject to availability of funding, start as soon as possibleJob DescriptionClinical Research Coordinator IV (JD0573)Faculty of Health Sciences | Department of Oncology | Trials Research and Clinical Evidence (TRACE) UnitMcMaster University's Faculty of Health Sciences leads health research and collaborates with academic hospital partners. TRACE focuses on clinical trial development and coordination across multiple sites.Job SummaryThe Clinical Research Coordinator leads regulatory coordination of clinical trials, develops training initiatives on Health Canada regulations and ICH Good Clinical Practice Guidelines, and manages daily operations of investigator-led trials.Primary Regulatory ResponsibilitiesSupport leadership, PIs, and collaborators in developing protocols and informed consent forms, ensuring safety and regulatory compliance.Apply research methodology appropriate for trial phases.Serve as primary liaison for Health Canada applications and provincial ethics board submissions.Facilitate the TRACE Safety Desk, oversee adverse event reporting to regulatory agencies and industry partners.Conduct internal audits and develop inspection readiness processes.Daily Operations of Multiple Clinical Research ProjectsDevelop implementation plans, manage timelines, estimate startup schedules,



and track milestones throughout the trial lifecycle.Plan and coordinate all aspects of trials across local and international sites.Implement quality assurance procedures, inspection guidelines, and educational resources.Coordinate data collection, entry, verification, and address challenges related to regulations such as GDPR.Write operational documents and compile reports for research groups and collaborators.Lead meetings with staff, PIs, industry collaborators, and external providers; report on trial status and regulatory updates.Additional SkillsOrganizational and detail-oriented.Project management and prioritization.Excellent oral, written communication; French language an asset.Teamwork and stakeholder engagement.Experience with Electronic Data Capture (EDC) and Clinical Trials Management System (CTMS).Facilitation and support of clinical trial personnel.Computer literacy with Office 365, online meeting platforms, and clinical trials systems.RequirementsMaster’s degree in a relevant field of study.6 years of relevant experience, including 1 year in a supervisory role.Additional RequirementsHybrid working model: in office 2 days per week (Wednesday/Thursday).Reliable home internet access.Pay Transparency StatementThe posted hiring range represents McMaster’s typical hiring range for this position. Actual salary will depend on experience, qualifications, internal equity, and market conditions.Employment Equity StatementMcMaster University is located on the traditional territories of the Haudenosaunee and Mississauga Nations. We value diversity, equity, and inclusion and welcome candidates from indigenous peoples, racialized communities, persons with disabilities, women, and the 2SLGBTQ+ community.#J-18808-Ljbffr

📌 Clinical Research Coord (Iv) - $42.0 - $59.1 An Hour (Winnipeg)
🏢 McMaster University
📍 Winnipeg