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, Positive 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.

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