Support hematology oncology clinical trials at Sunnybrook’s Bayview campus using informed consent, patient assessment, and clinical research expertise in office weekdays.

As a Clinical Research Associate I, you will maintain active oncology studies, databases, and trials within the Hematology Oncology Disease Site Group. You will report to the Physician Site Lead, Supervisor, and principal investigators. The work includes patient-facing activities, protocol application, trial documentation, and coordination with interdisciplinary teams, hospitals, sponsors, and contract research organizations.

Key Responsibilities:

- Consent patients and review eligibility criteria and medical records
- Apply protocols to medical histories, medications, adverse events, and reporting
- Conduct appointments, questionnaires, vital signs, ECGs, and measurements




- Process specimens and resolve sponsor queries through accurate data entry
- Maintain trial files and support trial activation, monitoring, and closure

Requirements:

- Health-related college diploma, certificate, or university degree
- Two to three years related experience, including one year clinical research
- Knowledge of ICH guidelines, Good Clinical Practice, and dangerous goods transportation
- Experience processing and shipping blood samples and obtaining informed consent
- Strong documentation, communication, analytical, organizational, and data-entry skills

Apply clinical research, patient communication, and protocol expertise to hematology oncology studies at Sunnybrook’s Bayview campus.

📌 Clinical Research Associate Hematology Oncology (Toronto)
🏢 Sunnybrook
📍 Toronto