Clinical Research Coordinator III - UHN, Toronto

AI Summary

This permanent full-time Clinical Research Coordinator III role at University Health Network (UHN) in Toronto, ON, focuses on Phase 1 clinical trials at Princess Margaret Cancer Centre. The position involves patient management, coordinating clinical studies for the Drug Development Program, and ensuring data collection. A Bachelor’s degree, current College of Nurses of Ontario registration, and 3-5 years of clinical experience are required. This critical role supports vital research advancements in patient care.

About the Clinical Research Coordinator III Role at UHN

As a Clinical Research Coordinator III at UHN's Princess Margaret Cancer Centre, you will play a pivotal role within the Cancer Clinical Research Unit (CCRU) Nursing department. This position involves close collaboration with Investigators and the healthcare team to manage and coordinate several clinical studies, primarily within the Phase 1 clinical trials group. Your responsibilities will include the recruitment of study participants, which involves identifying and screening potential subjects and obtaining informed consent. You will also coordinate patient visit schedules as per study protocol, executing all aspects of the study visit, including the assessment of adverse events, monitoring patient safety, and managing medication. The role requires meticulous sample collection, processing, and shipment according to clinical protocol, alongside vital signs, ECGs, and the administration of treatments. Providing direct clinical care for patients participating in these vital research trials is a core component, ensuring the implementation and coordination of all data collection and source documentation in line with UHN policy and ICH/GCP guidelines. This critical research position supports the Drug Development Program, contributing significantly to advancements in patient care.

Qualifications and Experience Required for This Research Position

To excel in this demanding yet rewarding clinical research position, candidates must possess a Bachelor’s degree or a recognized equivalent, coupled with a current certificate of competence (licensure/registration) from a college legislated under the Regulated Health Professions Act. Current registration with the College of Nurses of Ontario is absolutely required, demonstrating your commitment to professional standards. A minimum of three to five years of clinical and/or professional experience is essential, providing a solid foundation for the complexities of Phase 1 clinical trials. Strong knowledge of Phase I Clinical Trials is a key requirement, alongside a demonstrated ability to apply the nursing process in planning, implementing, and evaluating patient care. Evidence of excellent physical assessment, psychosocial assessment, and patient/family teaching skills is also required. While not strictly mandatory, recognized certification in clinical research (ACRP or SOCRA) is highly preferred, or a clear plan to work towards it. Chemotherapy certification from deSouza Institute is also an asset. Furthermore, excellent organizational and time management skills are required, as is the ability to work independently with accuracy in a dynamic research environment. Strong analytical, problem-solving, and interpersonal communication skills are critical for effective collaboration within the UHN team and with study participants. Attention to detail and meticulous documentation practice are paramount for maintaining the integrity of every study.