Clinical Research Coordinator III (PK)

Union: Non-Union Number of Vacancies: 3 New or Replacement Position: New Site: Princess Margaret Cancer Centre  Department: Cancer Clinical Research Unit (CCRU) Nursing Reports to: Clinical Research Nurse Manager Salary Range: $86,678 - $108,362 Per Year Hours: 37.5 Hours Per Week Shifts: Monday to Friday, and occasional Saturdays Status: Permanent Full-time  Closing Date: November 11, 2026 (Repost) Position Summary: The Clinical Research Coordinator collaborates with Investigators and health care team to assume responsibility for the overall patient management and coordination of several clinical studies for the Drug Development Program at Princess Margaret Cancer Centre. Studies include pharma-sponsored, cooperative group sponsored (such as NCIC) as well as Investigator initiated trials.  Duties: • Coordination of patient activities such as sample collection including processing and shipment of samples according to clinical trials protocols • Assessments, vital signs, ECG’s, monitoring and administration of treatments as per study protocol • Assists the primary Clinical Research Coordinator III with clinical care for patients participating in clinical trials and the implementation and coordination of all aspects of data collection and source documentation, as per UHN policy and ICH/GCP guidelines • Bachelor’s degree, or recognized equivalent, and current certificate of competence (licensure/registration) from a college legislated under the Regulated Health Professions Act, required • Registered Nurse with a minimum of 3 (three) years experience. • Excellent phlebotomy, IV and CVL skills • CNA certification in Oncology preferred • deSouza Chemo/Bio certification preferred • Excellent organizational and time management skills required • 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 • Autonomous clinical critical thinking ability • Recognized certification in clinical research (ACRP or SOCRA) obtained or plans to work towards. • Knowledge of IATA shipping regulations and basic laboratory procedures an asset • Minimum one (3) year clinical experience in oncology with strong knowledge base • Previous clinical research experience preferred • Training in ICH/GCP guidelines an asset. • 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 and Excel desired. 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 and promotions within a large organization • Additional perks (multiple corporate discounts including: travel, restaurants, parking, phone plans, auto insurance discounts, on-site gyms, etc.) Current UHN employees must have successfully completed their probationary period, have a good employee record along with satisfactory attendance in accordance with UHN's attendance management program, to be eligible for consideration. All applications must be submitted before the po