CRA II (Ontario)

<strong>Piper Companies</strong> is seeking a <strong>Clinical Research Associate </strong>for globally renowned CRO in <strong>Toronto, Ontario</strong>. This <strong>Clinical Research Associate </strong>must be located in Canada and have oncology experience. <strong>This is a remote position with on-site visits around Toronto, Ontario.<br><br></strong><strong>Responsibilities of the Clinical Research Associate</strong>:<br><br><ul><li>Conduct site monitoring visits following regulatory and contracted requirements.</li><li>Communicate progress reports to client and trial managers.</li><li>Work with sites on their recruitment plans, evaluating study quality, and administer study trainings.</li><li>Monitor site progress by reviewing submissions, approvals, recruitment, and enrollment.</li><li>Make sure site documents are available and up to date.<br><br></li></ul><strong>Qualifications for the Clinical Research Associate</strong>:<br><br><ul><li>1-4 years of experience as an on-site monitor.</li><li>Oncology experience required (1+ year experience preferred).</li><li>Familiarity with FDA, GCP, ICH, and similar local regulations.</li><li>Bachelor's degree required. <br><br></li></ul><strong>Compensation for the Clinical Research Associate:<br><br></strong><ul><li>Salary Range: 100,000-120,000/year CAD</li><li>Comprehensive Benefits: Sick leave if required by law, medical, dental, vision, 401K<br><br></li></ul><strong><em>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.<br><br></em></strong><strong>Keywords</strong>: 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.<br><br>