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Winnipeg Regional Health Authority
Overview
Responsible for the clinical analysis and reporting of patient samples according to established protocols. Assists with general laboratory projects, including SOPs and chemical inventories, while ensuring compliance with accreditation standards.
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Compensation
CA$39 - CA$49 / HOUR
Posted
2 days ago
Responsible for the clinical analysis and reporting of patient samples according to established protocols. Assists with general laboratory projects, including SOPs and chemical inventories, while ensuring compliance with quality assurance and accreditation standards.
WELL Health Technologies Corp
The role involves coordinating laboratory operations, managing supply chains, and performing sample accessioning and documentation review. Additionally, it requires performing method validation and biostudy analysis to generate analytical results in compliance with regulatory standards.
CA$40,000 - CA$40,000 / YEAR
Antech
The role is responsible for the identification, verification, processing, and preparation of microbiology samples. Key duties include performing quality controls, maintaining a clean workspace, and ensuring productivity goals are met.
CA$20 - CA$20 / HOUR
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.
Salary not listed
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.
The General Duty Medical Laboratory Technologist is responsible for performing clinical analysis on patient samples and reporting results according to established protocols. They also assist with laboratory projects such as maintaining SOPs and chemical inventories while ensuring compliance with safety and accreditation standards.
5 days ago
Responsible for the clinical analysis and reporting of patient samples according to established protocols. Additionally, assists with general laboratory projects, SOPs, and maintaining compliance with accreditation and quality assurance standards.
7 days ago
CA$56,818 - CA$56,818 / YEAR
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.
I R C M
Provide daily care, feeding, and health monitoring for laboratory animals while maintaining a clean and compliant facility. Perform cage changes, equipment sterilization, and basic technical treatments in accordance with biosafety protocols.
9 days ago
10 days ago
Syneos Health
The Analytical Scientist I provides support for the routine analysis of biological samples and ensures all activities follow company policies and SOPs. Responsibilities include processing samples, documenting results, and assisting with laboratory maintenance and waste disposal.
Cambridge Memorial Hospital
Perform a variety of complex laboratory tests and procedures while ensuring instruments are maintained and quality control standards are met. Support the laboratory Quality Management System and assist in the training of staff and students.
CA$37 - CA$50 / HOUR
11 days ago
The Medical Laboratory Technologist is responsible for performing clinical analysis and reporting on patient samples according to established protocols. They also assist with laboratory projects such as maintaining chemical inventories and ensuring compliance with safety and accreditation standards.
15 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
