Senior CRA / CRA II

ICON; Montreal; On-site; CAD 60,000 - 85,000; Full time

Job summary

A leading healthcare intelligence and clinical research organization based in Montreal is seeking a Clinical Research Associate (CRA). In this role, you will monitor clinical studies, ensuring adherence to protocols and regulations, while supporting better healthcare outcomes. Candidates must have a relevant undergraduate degree and experience in clinical monitoring, with a commitment to inclusivity and innovation.

Benefits

Competitive salary

Variable pay

Recognition programs

Benefits supporting well-being and work-life balance

Qualifications

• At least 1 year of clinical monitoring experience for level 2; 3+ years for level 3.
• Ability to travel up to 70%.
• Applicants must be authorized to work in the US or Canada.

Responsibilities

• Monitor clinical study progress at investigative sites or remotely.
• Ensure compliance with protocol, SOPs, ICH-GCP, and regulatory standards.

Skills

Clinical monitoring

Knowledge of ICH and local regulations

Oncology monitoring

Education

Undergraduate degree in clinical, science, or health-related field

Job description

Senior CRA / CRA II

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

Overview:

ICON plc is a global leader in healthcare intelligence and clinical research. We advance clinical research from molecule to medicine, providing outsourced services to pharmaceutical, biotechnology, medical device, and government/public health organizations.

With our patients at the center of all we do, we help accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, at the core of our culture, and the driving force behind our success. ICON employees are committed to success and passionate about doing their best.

Job Description

As a Clinical Research Associate (CRA), you will monitor the progress of clinical studies, either at investigative sites or remotely, ensuring trials are conducted, recorded, and reported according to protocol, SOPs, ICH-GCP, and regulatory requirements.

Responsibilities:

• Monitor clinical study progress at investigative sites or remotely.
• Ensure compliance with protocol, SOPs, ICH-GCP, and regulatory standards.

Qualifications:

• Undergraduate degree or equivalent in a clinical, science, or health-related field, or licensed healthcare professional, or equivalent experience.
• At least 1 year of clinical monitoring experience for level 2; 3+ years for level 3.
• Preferred experience in oncology monitoring.
• Ability to travel up to 70%.
• Knowledge of ICH and local regulations regarding drug trials.

Applicants must be authorized to work in the US or Canada without future sponsorship.

Benefits:

We offer a comprehensive package including competitive salary, variable pay, recognition programs, and benefits supporting your well-being and work-life balance. ICON is committed to inclusivity and equal opportunity employment.

If you require accommodations during the application process due to a disability or medical condition, please inform us.