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 environment 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 collaborative 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
- Robust 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