Lead clinical trial activities for UBC Cardiology, using Positive Clinical Practice, informed consent, and patient safety expertise. Collaborate with investigators and sponsors.

As a Clinical Research Nurse, you will work under Principal Investigators and the Research Manager in the Division of Cardiology. You will develop and supervise trials, promote multicentre research, and coordinate study work with hospital staff, researchers, and sponsors. Responsibilities include ethical submissions, regulatory documents, data collection, interim reporting, participant follow-up, and oversight of study conduct. The position supports local and international research activities while maintaining clinical and regulatory standards.

Key Responsibilities:

- Develop and implement clinical trials across research settings
- Prepare ethical, regulatory,



and hospital approval documents
- Design data collection methods, instruments, and databases
- Generate progress and interim reports for presentation
- Serve as liaison among investigators, sponsors, and research managers

Requirements:

- Ability to review and implement research protocols
- Knowledge of regulatory and ethical clinical trial standards
- Ability to coordinate data and specimen transfers
- Ability to analyze preliminary study data
- Ability to meet academic and industry sponsor deadlines

Bring clinical trial coordination, regulatory documentation, and sponsor liaison skills to UBC’s Division of Cardiology research program.

📌 Clinical Trials Nurse UBC Cardiology (Vancouver)
🏢 The University of British Columbia
📍 Vancouver