CRA II (British Columbia)

Piper Companies; Vancouver; Hybrid; CAD 100,000 - 120,000; Full time

Job summary

A clinical research organization is seeking a Clinical Research Associate II in Vancouver, Canada, responsible for monitoring clinical trials and ensuring protocol compliance. Candidates should have 1-4 years of oncology-related monitoring experience and a bachelor's degree. This remote position involves local site visits in British Columbia. Competitive salary offered between CAD 100,000 to 120,000 per year with comprehensive benefits.

Benefits

Medical benefits

Dental benefits

Vision benefits

401K

Sick leave

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.

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.

Skills

Oncology experience

Site monitoring

Regulatory compliance

Study training administration

Education

Bachelor's degree

Job description

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

Responsibilities of the Clinical Research Associate II

• 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 for the Clinical Research Associate II

• 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 for the Clinical Research Associate II

• 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, Vancouver, 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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