Clinical Research Coordinator III (Nurse - Phase 1) at University Health Network (UHN) in Toronto, ON

Job description

Union: Non-Union Number of vacancies: 1 New or Replacement Position: Replacement Site: Princess Margaret Cancer Centre  Department: Cancer Clinical Research Unit (CCRU) Nursing- Research Reports to: Director, Regulated Health Professionals Hours: 37.5 Hours Per Week Wage Range:  $86,678 - $108,362 Per Year Shifts: Monday to Friday Status: Permanent Full-Time Closing Date: December 1, 2026 Position Summary: The role of nursing in clinical trials continues to evolve as a growing profession within nursing.  It expands the nurse’s knowledge base, professional practice, autonomy and utilizes key elements of nursing practice such as patient assessment, 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 in the Phase 1 clinical trials group. Studies include pharma-sponsored, cooperative group sponsored (such as NCIC) as well as Investigator initiated trials. 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 of adverse events, monitoring safety, medication, questionnaires, sample collection, including processing and shipment of samples according to clinical protocol) 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 and ICH/GCP guidelines. Other study related activities, as needed.  Registered Nurse with a minimum of 3 to 5 years clinical and/or professional experience Current registration with the College of Nurses of Ontario Bachelor’s degree, or recognized equivalent, in a health or science-related discipline, required  Strong knowledge base in Phase I Clinical Trials Recognized certification in clinical research (ACRP or SOCRA) obtained or plans to work towards Some experience in research contract budget management Attention to detail and meticulous documentation practice Demonstrated knowledge and ability to utilize the nursing process in planning, implementing and evaluating patient care Evidence  of good physical assessment, psychosocial assessment and patient/family teaching skill Previous clinical research experience preferred Autonomous clinical critical thinking ability Training in ICH/GCP guidelines an asset Knowledge of IATA shipping regulations and basic laboratory procedures an asset Excellent organizational and time management skills required Strong analytical and problem solving skills Excellent interpersonal, verbal and written communication skills required Ability to set priorities and work independently with accuracy in a dynamic environment Proficiency with MS Office software – Word, Excel and Power Point preferred. Why join UHN? In addition to working alongside some of the most talented and inspiring healthcare professionals in the world, UHN offers a wide range of benefits, programs and perks. It is the comprehensiveness of these offerings that makes it a differentiating factor, allowing you to find value where it matters most to you, now and throughout your career at UHN. Competitive offer packages Government organization and a member of the Healthcare of Ontario Pension Plan (HOOPP https://hoopp.com/ ) Close access to Transit and UHN shuttle service A flexible work environment Opportunities for development