Make an impact at UHN as a Clinical Study and Regulatory Specialist I in the Tumor Immunotherapy Program, fostering innovation in cancer treatment through clinical trials and regulatory compliance. As Canada’s leading research hospital, UHN offers a unique workplace at the Princess Margaret Cancer Centre for you to engage in pioneering oncology research. In this 19-month contract, you will ensure compliance for clinical trials, maintaining high data integrity and quality standards within a cooperative team of specialists.

Key Responsibilities:
Prepare and submit regulatory documents to authorities
Promote the integrity of clinical trial data collection
Ensure adherence to ICH-GCP, FDA and Tri-Council regulations




Manage study-related documentation and administrative tasks
Maintain study trackers and training logs systematically Requirements:
Bachelor’s degree in Health or Science-related field
Minimum 2 years' experience in oncology research
At least one year in regulatory submissions
Proficiency in written and verbal communication
Solid organizational skills and attention to detail Contribute your expertise to transform patient care through research at UHN, and support cutting-edge therapies in oncology.

📌 Uhn Clinical Research And Regulatory Role Toronto
🏢 University Health Network
📍 Toronto