Oncology CRA - Remote Canada, Flexible Hours

Translational Research in Oncology; Canada; Hybrid; CAD 146,000 - 194,000; Full time

Benefits offered by this job

Competitive salary

3 weeks vacation

2 weeks leave

Insurance package

Flexible hours

Internet allowance

RRSP match 5%

Job summary

Translational Research in Oncology (TRIO) is seeking an experienced CRA for the Monitoring Resources team. This home-based Canadian role reports to a CRA Line Manager and supports oncology clinical trials across sites from Canada.

Responsibilities include site visits, regulatory document handling, data verification, and ensuring FDA/ICH-GCP compliance. Travel up to 60% and collaboration within a skilled team are expected.

Qualifications

• Minimum 2 years of oncology trial monitoring experience.
• Fluent in English and French.
• Experience monitoring Phase I studies.
• Advanced knowledge of oncology.
• Bachelor's degree in a science-related field.
• Strong knowledge of medical terminology and clinical monitoring processes.
• Solid knowledge of ICH-GCP guidelines.
• Familiarity with clinical trial information systems.
• Ability to travel up to 60% on average.

Responsibilities

• Conduct site visits (pre-study, initiation, monitoring, termination).
• Ensure adherence to FDA, ICH-GCP and local regulations.
• Collect and finalize regulatory documents.
• Verify data against source documents.
• Ensure compliance with FDA/ICH-GCP guidelines.
• Assist with budget negotiations and follow-up where applicable.
• Support data validation and resolve queries.
• Mentor junior team members as needed.

Skills

Oncology trial monitoring

ICH-GCP knowledge

Medical terminology

Clinical trial systems

Education

Bachelor's degree in science

Tools

CTMS

Job description

Translational Research in Oncology (TRIO) is seeking an experienced CRA for the Monitoring Resources team. This home-based Canadian role reports to a CRA Line Manager and supports oncology clinical trials across sites from Canada.

Responsibilities include site visits, regulatory document handling, data verification, and ensuring FDA/ICH-GCP compliance. Travel up to 60% and collaboration within a skilled team are expected.