Clinical Research Coordinator III (PK)
Core
Coordinate patient management and clinical studies for the Drug Development Program, including sample collection, treatment administration, and data collection.
Role type
Senior Clinical Research Coordinator (Oncology)
Builds
Clinical trial data and patient care outcomes for pharma-sponsored and investigator-initiated trials
Domain
Healthcare / Oncology / Clinical Research
Required skills
Phlebotomy, IV insertion, Central Venous Line (CVL) management, Patient assessment, Vital signs monitoring, ECG interpretation, Data collection, Source documentation, ICH/GCP guidelines knowledge, Laboratory procedures
Preferred skills
Oncology CNA certification, deSouza Chemo/Bio certification, Clinical research certification (ACRP/SOCRA), IATA shipping regulations knowledge
Technologies
MS Office (Word, Excel)
Responsibilities
Coordinate patient activities including sample collection and shipment; Perform assessments, vital signs, ECGs, and administer treatments per protocol; Assist with clinical care and data collection for trial patients; Ensure compliance with UHN policy and ICH/GCP guidelines
Seniority
Mid-Senior, hands-on IC