Clinical Research Associate

ICON Strategic Solutions; Canada; On-site; CAD 60,000 - 80,000; Full time

Job summary

A leading clinical research organization in Canada is seeking a Clinical Research Associate (CRA) to conduct site visits, ensure protocol compliance, and collaborate with investigators. Candidates should have a Bachelor's degree in a scientific field and at least 2 years of experience in clinical research. Strong communication skills and attention to detail are essential. This position offers the opportunity to contribute to high-quality clinical trials.

Qualifications

• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensure protocol compliance, data integrity, and patient safety throughout the trial.
• Collaborate with investigators and site staff to facilitate study conduct.
• Perform data review and resolution of queries to maintain high-quality clinical data.
• Contribute to preparation and review of study documentation.

Skills

Organizational skills

Communication skills

Detail-oriented

Knowledge of clinical trial processes

Education

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

Job description

As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What you will be doing

• 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, including protocols and clinical study reports

You Are

• Bachelor's degree in a scientific or healthcare-related field is highly preferred.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.