Remote Clinical Research Associate in Oncology

Advance your career with TRIO as a Remote Clinical Research Associate, joining the Monitoring Resources team in Western Canada. Engage in vital clinical trials and support transformative cancer treatments.

TRIO is actively seeking a Clinical Research Associate to be a part of its dynamic Monitoring Resources team. You will conduct site visits, ensure compliance with regulations, and validate critical data across clinical trials. This role calls for a minimum of two years of CRA experience, particularly in monitoring phase 1 trials, and offers the flexibility of remote work.

Key Responsibilities:

• Conduct site visits, including monitoring and termination

• Confirm adherence to FDA, ICH-GCP, and local regulations

• Collect and complete necessary regulatory documents

• Verify source documents and ensure data integrity

• Mentor junior team members and assist with budget negotiations

Requirements:

• Bachelor’s Degree in allied health fields required

• Minimum of 2 years CRA experience necessary

• Strong knowledge of clinical monitoring processes

• Ability to travel up to 60% for site visits

• Fluent in English;
French preferred

Elevate your expertise in oncology research while making a significant impact at TRIO.