Union: Non-Union
Site: Toronto General Hospital/ Princess Margaret Cancer Centre
Department: Department of Medical Oncology
Reports to: Nurse Manager, Clinical Trials DMOH
Work Model: On-Site
Grade: D0:08
Hours: 37.5 hours per week
Salary: $82,310 -- $102,882 annually (To commensurate with experience and consistent with UHN compensation policy)
Shift: Monday - Friday
Status: Permanent Full-Time
Closing Date: May 22, 2025
Position Summary:
The role of nursing in clinical trials continues to evolve as a growing subspecialty of oncology nursing. It expands the nurse's knowledge base, professional practice, autonomy and utilizes key elements of nursing practice such as patient assessment, documentation, critical thinking and holistic patient care. What is unique to this role is that all of these functions are within the realm of clinical trials. If you are looking for a challenging nursing role that is both rewarding and interesting, we may have that role for you.
The Clinical Research Coordinator III collaborates with Investigators and the health care team to assume responsibility for the overall patient management and coordination of several clinical studies for the Department of Medical Oncology at Princess Margaret Hospital. The research nurse will work primarily with the Blood Disorders Program site team with the opportunity to float in future to another site as needed.
Duties:
- Recruitment of study participants (e.g. identify and screen potential subjects, obtain informed consent);
- Coordination of patient visits schedules as per study protocol;
- Execution of all aspects of study visit (e.g. assessment adverse events, monitoring safety, medication, questionnaires, sample collection),provides clinical care for patients participating in clinical trials and the implementation and coordination of all aspects of data collection and source documentation within required timeframes, as per UHN policy, regulatory requirements and ICH/GCP guidelines.
