Compensation: CAD 75000 - CAD 95000 - yearly

Company Description
Traferox creates, manufactures and commercializes products for organ transplantation (lungs, heart, liver, kidneys, pancreas). These products employ technologies invented by transplant surgeons at partnering institutions, translating impactful clinical innovations into new standards of care. Traferox currently markets the TorEx Lung Perfusion System and the XPort Lung Preservation System and is committed to improving transplant outcomes and saving patients’ lives.

Location:

The work will be performed in the company’s place of work at 2400 Skymark Ave. Unit 3, Mississauga, Ontario L4W 5K5.This role may require some travel to clinical sites ( Union: Non-Union
Number of Vacancies: 1
New or Replacement Position: New
Site: 2400 Skymark Avenue,Mississauga
Department: Clinical
Reports to: Clinical Operations Manager
Salary Range: $75,000 - $95,000 annually
Hours: 37.5 Hours Per Week
Shifts: Days,Monday - Friday
Status: Permanent Full-time
Closing Date: August 19, 2026

Position Summary:

The Clinical Research Associate will support the end-to-end execution of clinical trials and post-market activities, ensuring studies are delivered in compliance with regulatory and company standards. The position supports trial start-up, conduct, and close-out. Through proactive communication, careful planning, effective management of timelines, and documentation, the successful candidate will help drive study progress and contribute to the delivery of high-quality clinical data. The role also involves collaborating with cross-functional teams to support the development and implementation of clinical research plans. This is a full time, in-person role based in Mississauga, ON, with travel to partnering clinical sites as needed.

Duties and Responsibilities:

Support on-site trial start-up, conduct and close-out activities in accordance with industry and company standards

Support clinical site interactions including assistance with REB/IRB applications, enrollment tracking,



CRF completion and issue resolution

Track enrollment, study milestones, and timelines, maintaining up-to-date status trackers and dashboards

Prepare and maintain key clinical documents including protocols, informed consent forms, site agreements, amendments, CRFs, monitoring plans, project plans, data plans, summary and annual reports

Maintain Trial Master Files in compliance with ICH-GCP, Tri-Council Guidelines, PHIPA, HIPAA, Health Canada/FDA regulations

Support data entry and query resolution in the EDC/eCRF system.

Participate in monitoring activities at clinical trial sites to assure adherence to GCP and ICH guidelines, regulatory requirements, SOPs, and confirm data completeness and accuracy

Contribute to regulatory submissions to Health Canada, FDA and under EU MDR

Collaborate with project specific committees such as DSMBs

Develop tools to ensure accurate data collection and data integrity

Travel as needed for site initiation and monitoring visits

Qualifications

Undergraduate degree in life sciences, health sciences, biomedical engineering, nursing, or a related field; a post-graduate degree in clinical research or a related field is an asset

Minimum of 1 year ofclinical research experience

Exposure to clinical trial design and data analysis

Strong analytical and problem-solving skills

Experience working with cross-functional teams and effective collaboration skills

Excellent oral and written communication skills

Solid organizational skills and high attention to detail with the ability to manage multiple deadlines at once

Additional Qualifications:

Training in GCP/ICH guidelines

Experience in biostatistics, data science, and/or data quality management

Experience drafting, and maintaining a TMF

Experience with site initiation visits, monitoring visit

Experience in healthcare, medical devices or biotechnology industry

Additional Information
We thank all applicants for their interest in this position with Traferox Technologies Inc. Please note that only candidates selected for an interview will be contacted.

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📌 Clinical Research Associate (Ontario)
🏢 UHN Research
📍 Ontario