UHN Clinical Research and Regulatory Role

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

• Strong organizational skills and attention to detail

Contribute your expertise to transform patient care through research at UHN, and support cutting-edge therapies in oncology.
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