Remote Clinical Research Associate - Oncology Trials

TRIO - Translational Research in Oncology; Vancouver; Remote; CAD 100,000 - 123,000; Full time

Benefits offered by this job

Annual compensation review

3 weeks vacation

10 days personal/sick time

1 paid volunteer day

Health, Dental, Vision & Life

RRSP Matching Program

Flexible working hours

Internet Allowance

Home Office Allowance

MaternityLeave Top-Up

Employee Assistance Program

Employee Referral Bonus

Job summary

TRIO - Translational Research in Oncology in Canada is seeking a Clinical Research Associate to join the Monitoring Resources team. This remote position supports Western Canada (BC/AB/SK/MB) and reports to the CRA Line Manager. The role involves site visits, regulatory compliance, data verification, and collaboration across teams.

You will work independently and as part of a team, travel up to 60%, and contribute to ongoing trial activities while upholding ICH-GCP standards and company policies.

Qualifications

• Bachelor's Degree in allied health fields such as Medical, Nursing, Pharmacy, or Health Science.
• Minimum 2 years of CRA experience.
• Experience monitoring phase 1 trials.
• Excellent knowledge of medical terminology and clinical monitoring process.
• Strong ICH-GCPs knowledge.
• Experience with clinical trial information systems.
• Ability to travel up to 60% on average.
• Must work both independently and in a team environment.
• Read, write and speak fluent English required; French desirable.

Responsibilities

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

Skills

Clinical monitoring

Regulatory compliance

Medical terminology

ICH-GCP

Trial information systems

Travel availability

Site visits

Education

Bachelor's degree in allied health fields

Tools

CTMS

Clinical trial processes

Job description

TRIO - Translational Research in Oncology in Canada is seeking a Clinical Research Associate to join the Monitoring Resources team. This remote position supports Western Canada (BC/AB/SK/MB) and reports to the CRA Line Manager. The role involves site visits, regulatory compliance, data verification, and collaboration across teams.

You will work independently and as part of a team, travel up to 60%, and contribute to ongoing trial activities while upholding ICH-GCP standards and company policies.