This job posting has expired
Expired on April 1, 2026
CRA I, Ontario
Job Description
ICON plc is a world-leading healthcare intelligence and clinical research organization. As a Clinical Research Associate (CRA), you will conduct clinical trial site visits including evaluation, initiation, monitoring, and close out. You will oversee and report on the conduct of clinical trials at a site level and ensure excellence in operational and scientific delivery.
Responsibilities
- Conduct clinical trial site visits including evaluation, initiation, monitoring and close out
- Oversee and report on the conduct of clinical trials at a site level
- Identify opportunities and best practices with local/regional partners
- Establishing and maintaining solid and professional relationships with site staff
- Verification of electronic case report form data against written and electronic source documentation
- Conducting IP accountability and reconciliation
Qualifications
- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Fluent oral and written English language skills
- Able and willing to travel up to 60% of the time
- Possession of a full driver’s license