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Vancouver Coastal HealthNew
Overview
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.
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Compensation
CA$41 - CA$56 / HOUR
Posted
New
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.
Nova Scotia Health and IWK Health
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
7 days ago
Fortrea
The role involves managing all aspects of clinical site monitoring, including initiation, routine visits, and close-out for oncology trials. Key duties include ensuring patient safety, verifying informed consent, and maintaining data integrity through CRF review and SAE reporting.
Salary not listed
9 days ago
Vancouver Coastal Health
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 reviewing research protocols, collecting biological samples, and maintaining accurate study documentation.
10 days ago
Rejuvenation
Coordinate all clinical trial activities in compliance with protocols and regulatory requirements. This includes recruiting participants, conducting research visits, and maintaining accurate study documentation using the RealTime CTMS system.
14 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
Syneos Health
The Research Nurse will be fully conversant with the trial protocol, ensuring accurate documentation, data transfer, and adherence to GCP throughout the study. Key duties include coordinating subject visits, administering trial medication, assisting with patient recruitment, and accurately reporting adverse events.
2 months ago
