Clinical Research Associate II (SRI) - Odette Cancer Centre Clinical Trials - Regular Full-time[...]

Sunnybrook; Toronto; On-site; CAD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a Clinical Research Associate II to join their dedicated team at the Odette Cancer Centre. This full-time role involves supporting oncology clinical studies, managing protocol tasks, and collaborating with various stakeholders to ensure high-quality research outcomes. The ideal candidate will have a strong background in clinical research, particularly in oncology, and possess excellent communication and organizational skills. This is a fantastic opportunity to contribute to groundbreaking cancer research in a supportive environment with comprehensive benefits.

Benefits

Health Benefits

Pension Plan

Paid Time Off

Qualifications

• 3-5+ years of clinical research experience, with a focus on oncology trials.
• Certifications such as SoCRA/CCRP are assets.

Responsibilities

• Assist with maintaining active oncology clinical studies and databases.
• Support patient-facing activities such as consenting and scheduling.

Skills

Clinical Research

Oncology Trials

Communication Skills

Organizational Skills

Teamwork

Education

Bachelor's Degree in Health or Science

Tools

Trial Management Systems

Job description

Clinical Research Associate II (SRI) - Odette Cancer Centre Clinical Trials - Regular Full-time 2025-13167 (2025-13167)

Join to apply for the Clinical Research Associate II (SRI) - Odette Cancer Centre Clinical Trials - Regular Full-time 2025-13167 (2025-13167) role at Sunnybrook.

Position Overview

The Odette Cancer Center (OCC) Clinical Research program, part of Sunnybrook Research Institute (SRI), is committed to high-quality clinical research. The program involves over 35 physicians and 55 staff across 12 disease site groups, including Breast, CNS, NETS, GI, GU, Gynecology, Head & Neck, Hematology, Lung, Melanoma, and Personalized Medicine, as well as two pan-Canadian initiatives.

Responsibilities

• Assist the Head & Neck Oncology Disease Site Group with maintaining active oncology clinical studies, databases, and trials.
• Support patient-facing activities such as consenting, reviewing eligibility, scheduling, and conducting measurements.
• Manage protocol activation tasks, including REB submissions, liaising with departments, and document management.
• Coordinate with CROs and sponsors, manage trial files, and support SIVs.

Qualifications

• Bachelor’s degree in health or science-related discipline with 3-5+ years of clinical research experience, including 3 years in oncology trials preferred.
• Certifications such as SoCRA/CCRP are assets.
• Knowledge of ICH guidelines, GCP, and trial management systems.
• Excellent communication, organizational, and teamwork skills.
• Experience with blood sample processing, protocol activation, and documentation.

Additional Details

This is a full-time, on-site position at Sunnybrook, Bayview campus, with benefits including health, pension, and paid time off. The candidate should be able to walk across campus as needed.

If qualified, please submit your resume with your name in the filename. Application screening will continue until a suitable candidate is found.