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University of Lethbridge
Overview
conduct research in genomics in health. attract research funding. build an internationally recognized research program. supervise graduate students and post-doctoral fellows. teach courses in biological sciences
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Compensation
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ICON plcNew
Serve as the primary contact between investigational sites and sponsors while conducting all types of site visits. Ensure site compliance with ICH-GCP and Health Canada regulations while managing data quality and patient safety reporting.
CA$108,576 - CA$135,720 / YEAR
New
AbCelleraNew
The role involves designing and executing in vitro and in vivo toxicology studies to assess the safety of drug candidates. Responsibilities include maintaining GLP-compliant data and authoring toxicology sections for regulatory documentation.
CA$100,000 - CA$125,000 / YEAR
Lead the design and oversight of in vitro and in vivo toxicology studies to assess the safety of drug candidates. Serve as a subject matter expert for nonclinical safety, authoring regulatory documentation and providing risk-benefit evaluations to leadership.
CA$112,000 - CA$150,000 / YEAR
Vancouver Coastal HealthNew
The Clinical Research Nurse provides direct clinical care and manages the screening, registration, and follow-up of participants in Phase 1 clinical trials. Responsibilities include collecting biological samples, performing diagnostic tests, and maintaining accurate study documentation in accordance with protocols.
CA$41 - CA$56 / HOUR
The Clinical Research Nurse provides direct clinical care and manages research participants through screening, registration, and ongoing follow-up according to study protocols. Responsibilities include collecting biological samples, performing diagnostic tests, and maintaining accurate study documentation and case report forms.
Fraser HealthNew
The Registered Nurse provides direct, person-centered care to acutely ill elderly patients through assessment, planning, and evaluation of nursing interventions. They collaborate with an interprofessional team to coordinate care, manage discharges, and educate patients and their families.
CA$41 - CA$60 / HOUR
University of British Columbia
The Research Coordinator manages day-to-day project activities, including patient recruitment, screening, and database management. They are also responsible for securing ethics approvals and supervising research assistants and students.
CA$4,567 - CA$5,386 / MONTH
2 days ago
ICON plc
Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with regulations. Oversee patient safety, drug accountability, and data quality while collaborating with cross-functional clinical teams.
CA$110,520 - CA$138,150 / YEAR
AstraZeneca
The CRA is responsible for monitoring study conduct at allocated sites to ensure proper delivery and compliance with international guidelines and local regulations. Key tasks include site initiation, monitoring visits, data verification, and managing study supplies and documentation.
CA$109,149 - CA$143,258 / YEAR
Nova Scotia Health and IWK Health
The CRA Nurse coordinates Children's Oncology Group clinical trial activities to ensure regulatory compliance and integration into clinical practice. Responsibilities include protocol feasibility review, data management, patient eligibility verification, and maintaining research charts.
CA$41 - CA$52 / HOUR
3 days ago
The Research Coordinator will manage day-to-day activities for GI research projects, including participant recruitment, interviews, and chart reviews. They are responsible for drafting ethics applications, performing data analysis, and preparing manuscripts and reports.
CA$39 - CA$46 / HOUR
4 days ago
Humber River Health
The Summer Student will support the Nephrology Research Program by assisting with systematic reviews and meta-analyses. Key tasks include protocol development, literature screening, data extraction, and report writing.
CA$20 - CA$20 / HOUR
The Research Assistant supports the Sekhon Laboratory by performing experiments, maintaining research databases, and assisting with knowledge translation via social media and websites. They also provide administrative support and collaborate with graduate students and the Principal Investigator.
CA$4,109 - CA$4,507 / MONTH
Jobgether
Serve as the primary contact for clinical trial sites to ensure protocol adherence and high-quality study execution from initiation to close-out. Conduct site visits and remote monitoring to maintain data integrity and ensure compliance with regulatory guidelines.
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.
CA$28 - CA$33 / HOUR
5 days ago
CHEO
The role involves receiving, verifying, and preparing clinical specimens for testing and shipping within a genetics program. Responsibilities include registering samples in the LIS, adhering to health and safety guidelines, and assisting in the instruction of medical laboratory students.
CA$32 - CA$39 / HOUR
CareAbout
The Clinical Research Nurse oversees the safety and consent of clinical trial participants while ensuring compliance with study protocols and GCP. Key duties include safety monitoring, administering investigational products, and maintaining emergency equipment records.
The Research Assistant supports study management by facilitating REB submissions, developing source documents, and maintaining organized filing systems. They are also responsible for participant recruitment, data entry into electronic Case Report Forms, and coordinating communications between participants and research staff.
CA$24 - CA$31 / HOUR
8 days ago
Hamilton Health Sciences
Oversees technical services and operations of animal research facilities, ensuring animal health and welfare. Supports the manager in coordinating equipment maintenance and adhering to institutional and legislative guidelines.
