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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.
ICON plcNew
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
AstraZenecaNew
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
2 days ago
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.
Salary not listed
3 days ago
University of British Columbia
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
4 days ago
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.
ICON plc
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
8 days ago
Indero
The Senior CRA monitors clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP guidelines. Responsibilities include conducting site visits, performing source data verification, and potentially mentoring other CRAs as a Lead CRA.
CAMH
The Coordinator integrates the voices of people with lived experience and family members into the planning, operations, and evaluation of research activities at CAMH. Key duties include facilitating patient-research partnerships, supporting the recruitment of patient advisors, and ensuring compliance with research ethics board requirements.
CA$38 - CA$51 / HOUR
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.
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
The Clinical Research Assistant will support research coordinators, investigators, and cross-functional teams in all phases of clinical trial execution, ranging from subject screening to data entry. Key duties include assisting with trial visits, collecting vital signs, making study-related calls, and documenting data accurately in electronic systems.
CA$54,000 - CA$58,000 / YEAR
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
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
Worldwide Clinical Trials
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
14 days ago
The Senior CRA conducts site qualification, initiation, monitoring, and close-out visits to ensure clinical trials adhere to protocols and regulatory standards. They also build relationships with investigators, perform source data verification, and may mentor other CRAs while overseeing site metrics.
16 days ago
