CRA II and Senior CRA

ICON plc; Montreal; On-site; CAD 60,000 - 80,000; Full time

Job summary

A leading global organization in clinical research is seeking a Clinical Research Associate (CRA) based in Montreal. The role involves monitoring clinical studies, ensuring compliance with protocols, and supporting the development of life-saving medicines. Bilingual candidates are preferred.

Benefits

Competitive compensation package

Benefits and social programs

Wellness initiatives

Qualifications

• 1+ years of clinical monitoring experience for CRA II, 3+ years for CRA III.
• Oncology monitoring experience preferred.

Responsibilities

• Monitor the progress of clinical studies at investigative sites or remotely.
• Ensure trials are conducted according to protocol, SOPs, ICH-GCP, and regulatory requirements.

Skills

Bilingual in English and French

Knowledge of ICH and local regulations

Education

Degree in a related field

Job description

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.

Overview:

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device, and government and public health organizations.

With our patients at the center of all that 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 people have a mission to succeed and a passion that ensures we do our work well.

Job Description / Description du Poste

ICON plc is a leading global organization in clinical research and health care intelligence. From molecule to medicine, we promote clinical research by offering outsourced services to pharmaceutical, biotech, and medical device companies, as well as government and public health agencies.

Keeping our patients at the center of all activities, we help accelerate the development of life-saving medicines and devices that improve quality of life.

Our employees are central to our culture and are the driving force of our success. ICON employees are committed to success, and their passion guarantees quality work.

Responsibilities / Responsabilités

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

Qualifications / Qualifications

What do you need to have? / Que devez-vous avoir?

• Degree in a related field or equivalent experience; licensed healthcare professional preferred
• 1+ years of clinical monitoring experience for CRA II, 3+ years for CRA III
• Oncology monitoring experience preferred
• Ability to travel 70%
• Knowledge of ICH and local regulations on drug trials
• Bilingual in English and French required

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

Benefits / Les avantages de travailler pour ICON

We develop our employees through continuous learning and offer a competitive compensation package, including benefits, social programs, and wellness initiatives to support you and your family throughout your career.

ICON is an inclusive employer offering equal employment opportunities. We consider all qualified candidates without discrimination based on race, color, religion, gender, sexual orientation, gender identity, national origin, disability, or veteran status.

If you need accommodations during the application process due to health or disability, please inform us.