Clinical Research Associate

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

Job summary

A leading clinical research organization in Canada is seeking an experienced Clinical Research Associate (CRA) to manage clinical trial processes. Responsibilities include conducting site visits, ensuring protocol compliance, and collaborating with investigators. The ideal candidate has at least 2 years of experience in a CRA role and a strong background in clinical trial regulations. This position offers a dynamic work environment with opportunities for career growth.

Qualifications

• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Ability to work independently and collaboratively in a fast-paced environment.

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, including protocols and clinical study reports.

Skills

Organizational skills

Communication skills

Attention to detail

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.