Remote CRA: Data Management & Monitoring

s i systems; Edmonton; Remote; CAD 100,000 - 123,000; Full time

Benefits offered by this job

Annual compensation review

3 weeks vacation plus December closure

10 days paid personal/sick time

1 paid volunteer day per year

Health, Dental, Vision & Life premiums

Job summary

Translational Research in Oncology (TRIO) is seeking a Clinical Research Associate to join our Monitoring Resources team. The role is remote based in Western Canada, with travel as needed, reporting to the CRA Line Manager.

The candidate will conduct site visits, ensure regulatory compliance, and support data verification and mentoring within a dynamic clinical research environment. Minimum 2 years CRA experience is required, with a Bachelor's in allied health fields.

Qualifications

• Bachelor's degree in allied health fields or international equivalent.
• Minimum 2 years of CRA experience.
• Fluent in English; French is preferred but not required.

Responsibilities

• Conduct site visits including pre-study, initiation, monitoring, and termination.
• Ensure adherence to FDA, ICH-GCP, and local regulations.
• Verify data against source documents and resolve queries.
• Mentor junior team members as required.
• Support budget negotiations and follow-up where applicable.

Skills

Medical terminology

Clinical monitoring process

ICH-GCP knowledge

Education

Bachelor's degree in allied health fields

Tools

Clinical trial information systems

Job description

Translational Research in Oncology (TRIO) is seeking a Clinical Research Associate to join our Monitoring Resources team. The role is remote based in Western Canada, with travel as needed, reporting to the CRA Line Manager.

The candidate will conduct site visits, ensure regulatory compliance, and support data verification and mentoring within a dynamic clinical research environment. Minimum 2 years CRA experience is required, with a Bachelor's in allied health fields.