Elevate patient care with the Clinical Research Coordinator Nurse role at the Centre for Innovative Medicine. Collaborate on clinical studies in oncology with a focus on patient management and safety.

Under the guidance of the Manager of Oncology Research, you will support clinical research studies at the RI-MUHC’s Oncology Department. This full-time role requires coordination of patient assessments, informed consent, and data collection, alongside essential safety monitoring and compliance tasks. You will engage with investigators while ensuring a seamless flow of information and patient care throughout the research process.

Key Responsibilities:
• Obtain informed consent and assess patient eligibility
• Maintain detailed logs and protocol documentation
• Monitor medication compliance and patient safety
• Coordinate data collection and source documentation
• Facilitate training and support for research protocols

Requ...