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University of British ColumbiaNew
Overview
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.
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Compensation
CA$4,567 - CA$5,386 / MONTH
Posted
New
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.
Salary not listed
4 days ago
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.
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
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
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
Bayshore
Administer and monitor specialized pharmacological treatments and investigational medicinal products in home, clinic, or community settings. Ensure strict adherence to clinical trial protocols, regulatory requirements, and accurate documentation of patient data.
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
Medison Pharma
The MSL is responsible for cultivating relationships with key opinion leaders and serving as the primary scientific contact between healthcare practitioners and Medison Medical Affairs. They deliver high-quality clinical presentations and communicate medical insights to refine overall medical strategy.
CA$130,000 - CA$150,000 / YEAR
14 days ago
Translational Research in Oncology
Responsible for processing and quality reviewing study documentation for the electronic Trial Master File (eTMF) according to SOPs and GCP guidelines. Provides administrative support to the TMF Manager through reporting, metrics, and document metadata assignment.
CA$37,000 - CA$41,000 / YEAR
15 days ago
hireVouch
Build new product features and systems from scratch across frontend and backend, directly expanding our platform capabilities for world-class researchers. Design, build, and own scalable backend services, APIs, and data pipelines that power the AI platform across the application, identity, data storage, and ML layers. Work within fast-moving sprint cycles to ship code quickly, contributing to production within your first few weeks. Collaborate with a cross-functional team of engineers, product managers, designers, and AI scientists to translate complex scientific workflows into high-performance software. Own features end-to-end from early development through production deployment, iteration, and scale — ensuring they deliver real value to researchers at leading pharma and biotech organizations
CA$200,000 - CA$200,000 / YEAR
University of British Columbia
The Research Assistant supports clinical trials in hematology by managing regulatory documents, processing blood samples, and maintaining research databases. They act as a primary liaison between the research team, ethics boards, and industry sponsors to ensure institutional standards are met.
CA$4,334 - CA$5,156 / MONTH
16 days ago
IQVIA
The CRA II monitors Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. Responsibilities include conducting site visits, training personnel, and managing site activities from start-up to close-out.
CA$84,000 - CA$170,900 / YEAR
17 days ago
ICON plc
The Clinical Research Associate will monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. They will also collaborate with cross-functional teams to manage data collection, site performance, and stakeholder relationships.
Centricity Research
The coordinator will manage clinical study visits, ensure participant safety, and handle recruitment and enrollment processes. They are also responsible for maintaining accurate study documentation and ensuring compliance with regulatory requirements and protocols.
The Research Nurse provides administrative and clinical support for clinical trials at the CCfV Challenge Unit. Responsibilities include conducting participant visits, administering investigational products, and ensuring compliance with regulatory standards and Good Clinical Practice.
CA$40 - CA$49 / HOUR
20 days ago
WELL Health Technologies Corp
Perform medical screening tasks including obtaining informed consent, recording medical histories, and collecting biological samples in compliance with study protocols. Responsible for accurate data entry, vital signs monitoring, and ensuring regulatory compliance with GCP and SOPs.
CA$50,000 - CA$54,000 / YEAR
Care Access
The Clinical Research Coordinator, RN conducts delegated clinical tasks and monitoring of research participants while ensuring strict adherence to Good Clinical Practices (GCP) and protocol compliance. Key duties involve patient coordination, obtaining informed consent, performing clinical procedures like blood draws and ECGs, and managing investigational products.
