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University of British Columbia
Overview
The coordinator manages operational tasks for industry-sponsored clinical trials and academic research within the Eczema Research and Care Program. Key duties include participant recruitment, data collection, regulatory ethics submissions, and coordinating study visits at BC Children's Hospital.
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Compensation
CA$28 - CA$33 / HOUR
Posted
4 days ago
Providence Healthcare
Coordinate clinical trials from start-up to closeout, supporting multiple Principal Investigators within a centralized research model. Manage participant recruitment, screening, and data integrity while ensuring strict adherence to regulatory and ethical standards.
CA$32 - CA$47 / HOUR
9 days ago
University of Alberta
The coordinator supports multiple industry-sponsored or grant-funded clinical trials from start-up to close-out. Key duties include managing ethics applications, regulatory documents, informed consent, and conducting study visits for data collection.
CA$56,627 - CA$76,909 / YEAR
Headlands Research
Research Assistants support the execution of clinical trials by assisting with study visits, preparing materials, and collecting data. They work closely with clinical teams to ensure studies run smoothly and in compliance with established protocols.
Salary not listed
Clinical Research Coordinators manage the day-to-day execution of clinical trials, including coordinating study visits and collecting data. They work directly with patients, investigators, and cross-functional teams to ensure compliance with protocols and regulatory requirements.
CA$45,000 - CA$100,000 / YEAR
Health Sciences North Research Institute
Oversee and manage clinical research studies across multiple portfolios from start-up to close-out. Coordinate day-to-day operations, data collection, and participant recruitment while ensuring regulatory compliance.
CA$31 - CA$37 / HOUR
11 days ago
Centricity Research
The coordinator will manage clinical study visits, ensure participant safety, and handle recruitment and enrollment processes. They are also responsible for maintaining accurate study documentation and ensuring compliance with regulatory requirements and protocols.
17 days ago
Care Access
The Clinical Research Coordinator, RN conducts delegated clinical tasks and monitoring of research participants while ensuring strict adherence to Good Clinical Practices (GCP) and protocol compliance. Key duties involve patient coordination, obtaining informed consent, performing clinical procedures like blood draws and ECGs, and managing investigational products.
20 days ago
Coordinate clinical studies by performing administrative and clinical tasks, ensuring participant safety and protocol compliance. Manage recruitment, screening, and data integrity while supporting monitoring visits and regulatory audits.
21 days ago
Inspired HR
The Clinical Research Coordinator leads multiple concurrent clinical trials, ensuring strict protocol adherence and high-quality data delivery. They manage the entire patient lifecycle from screening and enrollment to follow-up assessments and data documentation.
22 days ago
ClinSurge Research
The coordinator manages clinical research studies by handling participant recruitment, consent, and data entry into EDC systems. They ensure strict compliance with GCP, Health Canada, and IRB regulations while collaborating with investigators and sponsors.
23 days ago
IQVIA
Coordinate clinical research studies by performing complex clinical procedures and managing subject well-being. Responsibilities include recruiting volunteers, administering study drugs, and ensuring data accuracy in accordance with protocols.
CA$40 - CA$50 / HOUR
25 days ago
The Clinical Research Dietician provides nutritional counseling and education to participants in dermatology, obesity, and metabolic clinical trials. They are responsible for implementing nutrition plans, monitoring participant adherence, and maintaining accurate regulatory documentation.
28 days ago
WELL Health Diagnostic Centres
Coordinate day-to-day clinical trial activities, including participant recruitment, data management, and regulatory submissions to the Research Ethics Board. Manage study visits, perform clinical assessments like vitals and sample collection, and liaise with sponsors and internal departments.
CA$100,000 - CA$120,000 / YEAR
1 month ago
The Clinical Research Coordinator will support study execution by performing clinical procedures, managing participant safety, and ensuring compliance with protocols and regulatory requirements. They will also handle recruitment, screening, and data documentation to maintain high standards of study integrity.
