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

Sunnybrook; Toronto; On-site; CAD 60,000 - 90,000; Full time

Job summary

An innovative clinical research program seeks a Clinical Research Associate II to support oncology studies. This full-time, on-site role involves maintaining clinical trials, ensuring compliance with protocols, and collaborating with a dedicated team of professionals. The ideal candidate will possess a relevant degree and significant experience in clinical research, particularly in oncology. This position offers a dynamic environment where your contributions will enhance patient care and advance medical research. Join a forward-thinking organization committed to impactful clinical research and enjoy comprehensive health benefits, pension, and paid time off.

Benefits

Health Benefits

Pension

Paid Time Off

Qualifications

• 3-5+ years of clinical or professional experience, including 3 years in clinical research.
• Certification such as SoCRA/CCRP is an asset.

Responsibilities

• Maintain active oncology clinical studies, databases, and trials.
• Conduct patient consenting, eligibility reviews, and monitor protocol requirements.

Skills

Clinical Research

Oncology Knowledge

Data Handling

Patient Communication

Organizational Skills

Attention to Detail

Education

Relevant Degree

Tools

Trial Documentation Management

Job description

Summary Of Duties And Responsibilities

The Odette Cancer Center (OCC) Clinical Research program, part of Sunnybrook Research Institute (SRI), is committed to high-quality, innovative clinical research. The program involves 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.

The Clinical Research Associate (CRA) II will support the Head & Neck Oncology Disease Site Group by maintaining active oncology clinical studies, databases, and trials. This full-time, on-site position at Sunnybrook, Bayview campus, offers health benefits, pension, and paid time off.

Primary responsibilities include patient consenting, reviewing eligibility, monitoring ongoing protocol requirements, adverse event reporting, scheduling, conducting measurements, liaising with hospitals, data entry, and specimen processing. Additionally, the CRA II will assist with protocol activation activities such as REB submissions, impact assessments, liaising with CROs and sponsors, managing trial documentation, and coordinating SIVs.

The role reports to the Site Lead and PIs and collaborates with the Clinical Trials Manager, Operations Manager, and other staff. The candidate should be a team player with a relevant degree and 3-5+ years of clinical or professional experience, including at least 3 years in clinical research, preferably in oncology or regulated trials. Certification such as SoCRA/CCRP is an asset. Skills required include knowledge of ICH guidelines, GCP, trial documentation management, data handling, and patient communication. The position requires organizational skills, attention to detail, and the ability to manage multiple priorities.