Temporary Clinical Trials & Regulatory Specialist I

University Health Network; Toronto; On-site; CAD 48,216 - 73,012; Full time

Benefits offered by this job

Competitive offer packages

HOOPP pension plan

Transit access

Flexible work environment

Development opportunities

Corporate discounts

Job summary

University Health Network (UHN) is seeking a Clinical Study and Regulatory Specialist for the Tumor Immunotherapy Program at Princess Margaret Cancer Centre. You will coordinate trials, prepare submissions to Health Canada and REB, and manage study documentation to ensure data quality and regulatory compliance.

The 19‑month temporary full‑time contract offers exposure to a leading cancer research program and opportunities to advance in clinical research within a large health system.

Qualifications

• Bachelor’s degree in Health or Science‑Related Discipline required.

Responsibilities

• Coordinate clinical trial activities from protocol review through to activation, follow up and closure.
• Prepare Health Canada and Research Ethics Board submissions.
• Maintain study trackers and regulatory documents; ensure data quality and compliance with ICH‑GCP, FDA and Tri‑Council regulations.
• Communicate effectively with stakeholders and support study staff in a fast‑paced environment.

Skills

Excellent communication

Organizational skills

Independent worker

Fast learner

Education

Bachelor’s degree in health or science-related discipline

Job description

University Health Network (UHN) is seeking a Clinical Study and Regulatory Specialist for the Tumor Immunotherapy Program at Princess Margaret Cancer Centre. You will coordinate trials, prepare submissions to Health Canada and REB, and manage study documentation to ensure data quality and regulatory compliance.

The 19‑month temporary full‑time contract offers exposure to a leading cancer research program and opportunities to advance in clinical research within a large health system.