Support gastrointestinal oncology trials at Sunnybrook’s Bayview campus through informed consent, protocol application, and patient-facing clinical research work. This full time weekday position is on-site.

As a Clinical Research Associate I, you will assist the GI Oncology Disease Site Group with active studies, databases, and trials. You will work with physicians, research staff, and interdisciplinary partners while reporting to the Physician Site Lead, Supervisor, and principal investigators. The work includes participant coordination, clinical measurements, specimen handling, documentation, and data management across oncology research activities.

Key Responsibilities:

- Review eligibility criteria and medical records with consenting patients
- Apply protocols to medical history, medications, adverse events, and reporting
- Schedule appointments, questionnaires, measurements, and specimen processing




- Enter data, resolve sponsor queries, and track trial metrics
- Maintain trial files and support trial activation, closure, and monitoring

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 blood samples and maintaining Trial Master Files
- Strong communication, organization, analytical thinking, and attention to detail

Apply clinical research, participant communication, specimen handling, and data skills within Sunnybrook’s GI oncology trials program.

📌 Clinical Research Associate Gastrointestinal Oncology (Canada)
🏢 Sunnybrook Health Sciences Centre
📍 Canada