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Nova Scotia Health and IWK Health
Overview
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.
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Compensation
CA$41 - CA$52 / HOUR
Posted
2 days ago
Bayshore
Deliver and monitor specialized infusion, injectable, or oral pharmacological treatments in home and clinic settings. Responsible for patient health assessments, IV access, and documenting adverse events according to pharmacovigilance requirements.
CA$36 - CA$45 / HOUR
ICON plc
Accountable for site selection and study start-up activities for Phase I-IV trials, ensuring timelines and deliverables are met. Manages regulatory submissions, site documentation, and financial contracts to achieve site greenlight.
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 Licensed Practical Nurse oversees the safety of clinical trial participants and maintains safety equipment in compliance with protocols and GCP. Key duties include performing safety assessments, blood collection, administering medication, and monitoring adverse events.
Johnson & Johnson Innovative Medicine
Develops and coordinates clinical and regulatory documents, including protocols and clinical study reports, within the oncology therapeutic area. Collaborates with cross-functional teams to establish document timelines and ensure adherence to internal standards and regulatory guidelines.
CA$74,000 - CA$119,600 / YEAR
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.
Deliver and monitor specialized infusion, injectable, or oral pharmacological treatments in home or clinic settings. Responsible for patient health assessments, IV access initiation, and documenting adverse events per pharmacovigilance requirements.
CA$35 - CA$40 / HOUR
6 days ago
Deliver and monitor specialized infusion, injectable, or oral pharmacological treatments in home and clinic settings. Responsible for patient health assessments, IV access management, and documenting adverse events per pharmacovigilance requirements.
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 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.
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.
9 days ago
Bruyère Health Research Institute
The role involves implementing and overseeing clinical research trials from feasibility to closeout, specifically focusing on brain and mind research. Key duties include administering investigational products, performing health assessments, and coordinating with pharmaceutical sponsors and investigators.
CA$34 - CA$39 / HOUR
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
Perform phlebotomy, specimen processing, and shipping in compliance with study protocols and safety regulations. Maintain detailed lab logs and support clinical trial operations through data entry and equipment calibration.
CA$52,000 - CA$58,000 / YEAR
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
