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 X°Port 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 (<10%).

Traferox Technologies Inc.

Union: Non-Union

Number of Vacancies: 1

New or Replacement Position: Current

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 in office 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 of clinical 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

Strong 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.

Compensation: CAD 75000 - CAD 95000 - yearly

📌 Clinical Research Associate (Mississauga)
🏢 University Health Network
📍 Mississauga