Bilingual Clinical Research Associate – Onsite Monitoring

ICON; Montreal; On-site; CAD 70,000 - 90,000; Full time

Job summary

A leading clinical research organization in Canada is seeking a Clinical Research Associate to manage clinical trials. The ideal candidate will have a Bachelor's degree, monitoring experience, and be bilingual in French and English. Responsibilities include conducting trial visits, ensuring compliance, and collaborating with site staff. Competitive salary and benefits are offered, focused on work-life balance.

Benefits

Various annual leave entitlements

Health insurance offerings

Retirement planning offerings

Employee Assistance Programme

Flexible optional benefits

Qualifications

• Minimum of 12 months onsite monitoring experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

Responsibilities

• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation.

Skills

Bilingual (French/English)

Strong organizational skills

Attention to detail

Communication skills

Ability to work independently

Ability to travel

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

A leading clinical research organization in Canada is seeking a Clinical Research Associate to manage clinical trials. The ideal candidate will have a Bachelor's degree, monitoring experience, and be bilingual in French and English. Responsibilities include conducting trial visits, ensuring compliance, and collaborating with site staff. Competitive salary and benefits are offered, focused on work-life balance.