Clinical Research Coordinator III (PK)

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: October 16, 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.

Employment type
Full-time

Work arrangement
No