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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.
University of British ColumbiaNew
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
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
The Memory ClinicNew
The Clinical Trial Associate manages regulatory tasks for Alzheimer's research trials, including IRB submissions and the maintenance of master files. They coordinate start-up activities and ensure ongoing compliance with ICH-GCP regulations and sponsor requirements.
CA$60,000 - CA$90,000 / 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
Fraser Health
Provide and coordinate pre- and post-procedure nursing care for patients in the Interventional Radiology unit. Responsibilities include conducting health assessments, assisting physicians during procedures, and managing procedural sedation and recovery.
CA$41 - CA$60 / HOUR
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
3 days ago
University of British Columbia
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.
Salary not listed
Provide comprehensive physiotherapy assessments, diagnoses, and evidence-based treatment plans for patients within an acute care setting. Collaborate with an interprofessional team to implement patient-centered care and manage discharge planning.
CA$45 - CA$56 / HOUR
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.
CHEO
Provide comprehensive psychological assessment and evidence-based treatment to youth and families within the Gender Diversity Program. Collaborate with an interdisciplinary team to conduct clinical research, program development, and supervise pre-doctoral interns.
CA$64 - CA$80 / HOUR
Sentrex Health Solutions
The role involves serving as a Research Coordinator and RPN to provide direct patient care and manage clinical trials in a dermatology setting. Key duties include administering medications, performing delegated medical acts, and coordinating patient access to specialized treatments.
CA$70,000 - CA$80,000 / YEAR
7 days ago
The Research Assistant supports the FORBOW study by assisting with participant recruitment, administering tests and interviews, and collecting biological samples. They are also responsible for study administration, data entry, and providing general administrative support.
CA$23 - CA$29 / HOUR
8 days ago
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.
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
