Manage oncology clinical trial data for Sunnybrook Research Institute on-site at the Bayview campus, using electronic data capture systems and databases.
This full time weekday position supports the GI Oncology Disease Site Group within the Odette Cancer Center Clinical Research program. You will maintain active studies while coordinating trial data, documentation, specimens, and communications. The work involves electronic data capture, medical information, monitoring visits, and trial activation.
Key Responsibilities: Collect and enter data into electronic systems and databases
Track patient visits, enrollment logs, and trial-related metrics
Resolve sponsor queries and support monitoring visits
Maintain trial master file documentation and complete forms




Communicate with participants, hospitals, sponsors, and CROs
Requirements: Health-related college diploma, certificate, or university degree
One to two years of related professional or practical experience
Knowledge of ICH guidelines, Good Clinical Practice, and dangerous goods transportation
Experience processing and shipping blood samples
Strong MS Office, organizational, communication, and analytical skills
Apply clinical research data, documentation, communication, and specimen-handling skills across Sunnybrook oncology trials.

#J-18808-Ljbffr

📌 Clinical Trials Data Coordinator (Ontario)
🏢 Sunnybrook Health Sciences Centre
📍 Ontario