Remote Oncology CRA — 1-Year Freelance Contract

Freelance; Vancouver; Remote; CAD 110,000 - 138,000; Full time

Job summary

Translational Research in Oncology (TRIO) is seeking a Clinical Research Associate to join the Monitoring Resource team. This is a remote, full-time freelance opportunity on a 1-year contract, open to candidates based in Western Canada (British Columbia, Alberta, Saskatchewan, or Manitoba).

Responsibilities include data verification, site visits (pre-study to termination), regulatory compliance, budget assistance, data validation, mentoring, and ensuring regulatory documents are completed.

Qualifications

• Minimum 3 years oncology experience as CRA/CRC/RN.
• At least 1 year monitoring in early-phase trials.
• Experience in solid tumor trials (breast, lung, gastric, ovarian, pancreatic) preferred.
• Fluent English; French desirable.
• Bachelor’s degree in a science-related field.
• Strong ICH-GCP knowledge and ability to travel up to 60%.

Responsibilities

• Perform data verification of source documents.
• Conduct site visits: pre-study, initiation, monitoring, termination.
• Ensure adherence to FDA, ICH-GCP and local regulations.
• Ensure implementation of FDA and ICH-GCP guidelines.
• Participate in budget negotiation and follow-up.
• Assist with data validation and query resolution.
• Mentor junior team members and collect regulatory documents.

Skills

Oncology CRA experience

Early-phase monitoring

Solid tumor trials

Fluent English

French desirable

Travel up to 60%

Legal work authorization

Medical terminology

ICH-GCP knowledge

Clinical trial systems

Education

Science-related Bachelor’s degree

Tools

Clinical trial information systems

Job description

Translational Research in Oncology (TRIO) is seeking a Clinical Research Associate to join the Monitoring Resource team. This is a remote, full-time freelance opportunity on a 1-year contract, open to candidates based in Western Canada (British Columbia, Alberta, Saskatchewan, or Manitoba).

Responsibilities include data verification, site visits (pre-study to termination), regulatory compliance, budget assistance, data validation, mentoring, and ensuring regulatory documents are completed.