Clinical Research Associate, Trials & Data Integrity

UHN Research; Mississauga; On-site; CAD 75,000 - 95,000; Full time

Job summary

Traferox Technologies Inc. in Mississauga is seeking a Clinical Research Associate to support end-to-end execution of clinical trials and post-market activities. You will help with trial start-up, conduct, and close-out, ensuring compliance with ICH-GCP, PHIPA and Health Canada requirements.

Based in Mississauga with some site travel (<10%), the role requires you to work cross-functionally, manage timelines, maintain TMFs, and contribute to regulatory submissions to Health Canada and FDA. A life sciences undergraduate degree and 1 year of clinical research experience are desired.

Qualifications

• Undergraduate degree in life sciences, health sciences, biomedical engineering, nursing, or related field.
• 1 year of clinical research experience is required.
• Exposure to clinical trial design and data analysis.
• Excellent written and oral communication and strong organizational skills.

Responsibilities

• Support on-site trial start-up, conduct and close-out activities in line with standards.
• Assist with REB/IRB applications, enrollment tracking, CRF completion and issue resolution.
• Track enrollment, milestones and timelines with up-to-date trackers and dashboards.
• Maintain TMF and key documents in compliance with GCP and regulations.
• Support data entry and query resolution in EDC/eCRF systems.
• Collaborate with cross-functional teams to support trial-related plans.
• Travel to clinical sites as needed for initiation and monitoring visits.

Skills

Analytical skills

Problem-solving

Communication skills

Organizational skills

Cross-functional collaboration

Education

Undergraduate degree in life sciences or related field

Post-graduate degree in clinical research (asset)

Job description

Traferox Technologies Inc. in Mississauga is seeking a Clinical Research Associate to support end-to-end execution of clinical trials and post-market activities. You will help with trial start-up, conduct, and close-out, ensuring compliance with ICH-GCP, PHIPA and Health Canada requirements.

Based in Mississauga with some site travel (<10%), the role requires you to work cross-functionally, manage timelines, maintain TMFs, and contribute to regulatory submissions to Health Canada and FDA. A life sciences undergraduate degree and 1 year of clinical research experience are desired.