Clinical Research Coordinator III; Phase Job Toronto area,Ontario Canada,Nursing

Position: Clinical Research Coordinator III (Phase 1)

Company Description

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.

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
Reports to: Clinical Research Nurse Manager
Salary Range: $84,779 - $105,968 Per Year
Hours: Hours Per Week
Shifts: Monday-Friday
Status: Permanent Full-time
Closing Date: August 14, 2026

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. 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 ( identify and screen potential subjects, obtain informed consent)

Coordination of patient visits schedules as per study protocol; execution of all aspects of study visit ( assessment adverse events, monitoring safety, medication, questionnaires, sample collection, including processing and shipment of samples according to clinical protocol, assessments, vital signs, ECG’s, monitoring and administration of treatments as per study protocol.

Provides 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.

Qualifications

Bachelor’s degree, or recognized equivalent, and current certificate of competence (licensure/registration) from a college legislated under the Regulated Health Professions Act

At minimum 3 to 5 years clinical and/or professional experience is required

Current registration with the College of Nurses of Ontario

Recognized certification in clinical research (ACRP or SOCRA) obtained or plans to work towards

Registered Nurse with a minimum of 3 (three) years experience

Strong knowledge base in Phase I Clinical Trials

Chemotherapy certification (de Souza Institute) is preferred

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

Training in ICH/GCP guidelines is 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…