Bilingual Clinical Research Associate

Embark on a career with Syneos Health as a Bilingual Clinical Research Associate in Toronto, ON. You'll ensure compliance with regulatory standards while managing clinical research site activities.

As a key member of our clinical team, you will perform site qualification, initiation, and monitoring for clinical trials.

Your role is critical in securing compliance with ICH-GCP and improving patient safety by protecting their confidentiality. Engage with passionate professionals focused on delivering impactful therapies globally.

Key Responsibilities:

• Perform regulatory compliant site qualifications and management

• Verify informed consent procedures are properly documented

• Conduct Source Document Reviews with attention to detail

• Oversee investigational product inventory and compliance

• Document project activities diligently for regulatory standards

Requirements:

• Bilingual proficiency (English and French)

• Relevant clinical monitoring experience required

• In-depth knowledge of ICH and GCP guidelines

• Strong organizational skills and attention to detail

• Ability to adapt to fluctuating project priorities

Utilize your monitoring expertise to support clinical trials and enhance patient safety at Syneos Health in Toronto.
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