CRA II and Senior CRA

ICON plc; Montreal; On-site; CAD 70,000 - 100,000; Full time

Job summary

ICON plc is seeking a CRA II or Senior CRA to join their team in Montreal. The role involves monitoring clinical studies, ensuring compliance with regulations, and requires a strong background in clinical monitoring. Bilingual candidates are preferred, and the company offers competitive salaries and comprehensive benefits.

Benefits

Annual leave entitlements

Health insurance options

Retirement plans

Employee Assistance Program

Flexible benefits based on country

Qualifications

• Minimum 1 year of clinical monitoring experience for CRA II; 3+ years for Senior CRA.
• Oncology monitoring experience preferred.
• Legally authorized to work in the US or Canada.

Responsibilities

• Monitor clinical studies at investigative sites or remotely.
• Ensure compliance with protocols, SOPs, ICH-GCP, and regulatory requirements.

Skills

Clinical monitoring

Bilingual (English/French)

Knowledge of ICH regulations

Education

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

Job description

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Talent Acquisition Business Partner at ICON plc

CRA II or Senior CRA - Home-based in Montreal (Bilingual French/English preferred)

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.

Job Overview

ICON plc is a global leader in healthcare intelligence and clinical research, advancing clinical studies from molecule to medicine. We provide outsourced services to pharmaceutical, biotech, medical device companies, and public health organizations.

Our focus is on accelerating the development of drugs and devices that save lives and improve quality of life, with our patients at the center of all we do.

Responsibilities

As a Clinical Research Associate (CRA), you will monitor clinical studies at investigative sites or remotely, ensuring compliance with protocols, SOPs, ICH-GCP, and regulatory requirements.

Qualifications

• Undergraduate degree or equivalent in a clinical, science, or health-related field, or licensed healthcare professional, or equivalent experience.
• Minimum 1 year of clinical monitoring experience for level 2; 3+ years for level 3.
• Oncology monitoring experience preferred.
• Ability to travel 70%.
• Knowledge of ICH and local regulatory regulations.
• Legally authorized to work in the US or Canada without sponsorship.

Additional Requirements

• Bilingual (English/French) required.
• Experience in oncology preferred.

Why Work at ICON

We invest in our employees' development through a culture of continuous learning. We offer competitive salaries, comprehensive benefits, and support work-life balance, including health insurance, retirement plans, and more.

ICON is committed to diversity and inclusion, providing equal opportunity employment and a workplace free of discrimination and harassment. Reasonable accommodations are available for applicants with disabilities.

What ICON Offers

Competitive salaries, benefits, and a supportive environment that values diversity and inclusion.

• Annual leave entitlements
• Health insurance options
• Retirement plans
• Employee Assistance Program
• Flexible benefits based on country

Visit our careers site for more information about our benefits.