Clinical Research Associate Bilingual Remote

Location: Lévis

Join a dynamic clinical team as a Bilingual Clinical Research Associate, conducting site management and monitoring remotely while ensuring compliance and data integrity. This role requires both regulatory knowledge and excellent communication skills.

As a Bilingual Clinical Research Associate, you will perform site qualification, initiation, and monitoring ensuring adherence to ICH-GCP and regulatory guidelines. Your expertise in Good Clinical Practice and attention to detail will be crucial in managing site activities while supporting subject recruitment. Effective communication with site staff and project teams will help you thrive in this role, where you may also mentor junior CRAs.

Key Responsibilities:

• Conduct site qualifications and manage monitoring visits

• Ensure regulatory compliance and investigate protocols

• Verify informed consent processes and documentation

• Support subject recruitment and retention strategies

• Document site activities and maintain accurate records

Requirements:

• Bachelor’s degree or RN in a related field

• Knowledge of ICH Guidelines and regulatory requirements

• Excellent communication and computer skills

• Ability to travel up to 75%

• Strong critical thinking skills

Leverage your bilingual skills and clinical expertise to drive impactful research at our organization.
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