CRA II (Ontario)

Piper Companies; Toronto; On-site; CAD 100,000 - 120,000; Full time

Job summary

A leading global CRO is seeking a Clinical Research Associate based in Toronto, Ontario. This remote position requires oncology experience and involves conducting site monitoring visits, communicating with clients, and ensuring regulatory compliance. Candidates should have at least 1 year of oncology experience, familiarity with FDA regulations, and a Bachelor's degree. Join a dynamic team focused on clinical trials and patient recruitment.

Benefits

Comprehensive benefits including medical, dental, and vision

401K

Sick leave if required by law

Qualifications

• 1-4 years of experience as an on-site monitor.
• Oncology experience required, with a preference for 1+ years.
• Familiarity with FDA, GCP, ICH, and similar local regulations.

Responsibilities

• Conduct site monitoring visits based on regulatory requirements.
• Communicate progress reports to client and trial managers.
• Work with sites on recruitment plans and administer training.
• Monitor site progress by reviewing submissions and approvals.
• Ensure site documents are up to date.

Skills

Oncology experience

Site monitoring

Regulatory compliance

Patient recruitment

Education

Bachelor's degree

Job description

Piper Companies is seeking a Clinical Research Associate for globally renowned CRO in Toronto, Ontario. This Clinical Research Associate must be located in Canada and have oncology experience. This is a remote position with on-site visits around Toronto, Ontario.

Responsibilities

• Conduct site monitoring visits following regulatory and contracted requirements.
• Communicate progress reports to client and trial managers.
• Work with sites on their recruitment plans, evaluating study quality, and administer study trainings.
• Monitor site progress by reviewing submissions, approvals, recruitment, and enrollment.
• Make sure site documents are available and up to date.

Qualifications

• 1-4 years of experience as an on-site monitor.
• Oncology experience required (1+ year experience preferred).
• Familiarity with FDA, GCP, ICH, and similar local regulations.
• Bachelor's degree required.

Compensation

• Salary Range: 100,000-120,000/year CAD
• Comprehensive Benefits: Sick leave if required by law, medical, dental, vision, 401K

This job opens for applications on 10/20/2025. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: CRA, Clinical Research Associate, oncology, Toronto, clinical trials, CRO, patient recruitment, FDA, GCP, ICH, on-site monitor, oncology clinical trial, site monitoring, protocol compliance, oncology trials, regulatory submissions, clinical site visits, clinical operations, study start up, clinical data review.

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