Coordinate clinical trial monitoring for ICON as a Bilingual Clinical Research Associate, applying medical data review and ICH-GCP knowledge. Travel approximately 60% as required.

As a CRA I, you will support clinical trial operations across ICON’s clinical programmes. The position involves study start-up and monitoring activities, accurate documentation, and collaboration with stakeholders. You will help deliver high-quality outcomes while supporting patient safety and regulatory compliance.

Key Responsibilities:

- Coordinate study setup and monitoring activities independently
- Complete accurate study status reports and maintain documentation
- Manage sponsor-generated queries and support cost efficiency
- Build relationships with investigators, stakeholders, and site staff
- Ensure compliance with procedures, protocols, and requirements

Requirements:

- University degree in medicine, science, or equivalent
- Clinical trial monitoring experience
- Knowledge of ICH-GCP guidelines
- Expertise reviewing and evaluating medical data
- Willingness to travel approximately 60% as required

Apply clinical monitoring, medical data review, and stakeholder collaboration skills as a bilingual CRA supporting ICON studies.

📌 Bilingual Clinical Research Associate (Canada)
🏢 ICON Strategic Solutions
📍 Canada