Clinical Research Nurse III - UHN, Toronto

AI Summary

This Clinical Research Coordinator III (Research Nurse) position at University Health Network (UHN) in Toronto, Ontario, involves supporting a diverse portfolio of clinical trials. The role focuses on providing high-quality clinical care to participants, coordinating study activities, and ensuring compliance with research regulations. Key requirements include being a Registered Nurse with the CNO, holding a Bachelor’s degree, and having experience with Epic for clinical documentation.

About the Clinical Research Nurse III Role at UHN

The University Health Network (UHN) is actively seeking a dedicated Clinical Research Coordinator III, often referred to as a Research Nurse, to join the dynamic team at the Toronto Western Hospital Clinical Research Unit. This pivotal role involves providing essential support for a diverse and expanding portfolio of clinical trials, spanning multiple therapeutic areas. The successful candidate will collaborate closely with investigators, fellow research staff, and interdisciplinary health care teams to ensure comprehensive patient management and the seamless coordination of various clinical research studies. This includes overseeing all aspects from study start-up to participant retention, ensuring that all clinical protocols are meticulously followed and that participants receive the highest standard of care throughout their study journey. The UHN is committed to advancing medical research, and this position is integral to that mission.

Key Responsibilities and Compliance in Clinical Research

A core responsibility of this clinical research position at UHN involves delivering high-quality clinical care to participants enrolled in trials. This encompasses a wide range of duties, including performing detailed clinical assessments such as vital signs, ECGs, and medical history collection, as well as administering investigational products and treatments strictly according to study protocols. The Research Nurse will also be crucial in monitoring participant safety, identifying and promptly reporting adverse events, and escalating any clinical concerns to the Most Responsible Physician as appropriate. Furthermore, the role requires meticulous coordination of biological sample collection, including processing and support for shipment, alongside screening and recruiting study participants. Obtaining informed consent and actively supporting participant retention through the study lifecycle are also key. Ensuring strict compliance with ICH Good Clinical Practice (GCP), Health Canada regulations, and UHN policies is paramount for all research activities.

Essential Qualifications for this UHN Opportunity

To excel in this clinical research role at UHN, candidates must be a Registered Nurse (RN) in good standing with the College of Nurses of Ontario (CNO) and possess a Bachelor’s degree or a recognized equivalent, along with a current certificate of competence. A minimum of two to three years of clinical experience, preferably in Neurology, is highly valued. The ability to effectively utilize the nursing process in planning, implementing, and evaluating patient care is essential, as is evidence of strong physical assessment, psychosocial assessment, and patient/family teaching skills. Proficiency in phlebotomy, IV insertion, and the operation of infusion pumps is required. While not mandatory, one to two years of clinical research experience and training in ICH/GCP guidelines are preferred assets. Knowledge of Transportation of Dangerous Goods regulations and basic laboratory procedures would also provide valuable support. Experience using Epic for clinical documentation and ordering is a mandatory requirement for this position. The successful candidate will demonstrate excellent organizational, communication, and problem-solving skills, coupled with the ability to work both independently and collaboratively within a fast-paced environment, providing support for multiple clinical trials.