Clinical Research Coordinator III; PK
UHN is Canada’s #1 hospital and the world’s #1 publicly funded hospital. With 10 sites and more than 44,000 TeamUHN members, UHN consists of Toronto General Hospital, Toronto Western Hospital, Princess Margaret Cancer Centre, Toronto Rehabilitation Institute, The Michener Institute of Education and West Park Healthcare Centre. As Canada's top research hospital, the scope of biomedical research and complexity of cases at UHN have made it a national and international source for discovery, education and patient care.
UHN has the largest hospital-based research program in Canada, with major research in neurosciences, cardiology, transplantation, oncology, surgical innovation, infectious diseases, genomic medicine and rehabilitation medicine. UHN is a research hospital affiliated with the University of Toronto.
UHN’s vision is to build A Healthier World and it’s only because of the talented and dedicated people who work here that we are continually bringing that vision closer to reality.
- Union: Non-Union
- Number of Vacancies: 1
- New or Replacement Position: Replacement
- Site: Princess Margaret Cancer Centre
- Department: Cancer Clinical Research Unit (CCRU) Nursing
- Reports to: Clinical Research Nurse Manager
- Salary Range: $84,779 - $105,968 Per Year
- Hours: 37.5 Hours Per Week
- Shifts: Monday to Friday, and occasional Saturdays
- Status: Permanent Full-time
- Closing Date: June 24, 2026
The Clinical Research Coordinator collaborates with Investigators and health care team to assume responsibility for 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, 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.
- de Souza 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.
In addition to working alongside some of the most talented and inspiring healthcare professionals in the world, UHN offers a wide range of…
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