Clinical Research Associate
Remote · Québec, Quebec, Canada
Job Summary
Clinical Research Associate responsible for site qualification, initiation, monitoring, and close-out visits; ensure protocol compliance, data integrity, and patient safety; collaborate with investigators and site staff; perform data reviews and resolve queries; contribute to preparation and review of study documentation including protocols and clinical study reports. The role requires a Bachelor's degree in a scientific/healthcare field, at least 9 months of onsite monitoring experience, strong knowledge of clinical trial processes and ICH-GCP, excellent organization and communication, ability to travel up to 60% and a valid driver's license, and the right to work in the role’s country.
Required Qualifications
- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 9 months onsite monitoring experience as a Clinical Research Associate (CRA I, CRA II, or Senior CRA)
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills
- Ability to work independently and collaboratively in a fast-paced environment
- Ability to travel at least 60% of the time (international and domestic) with a valid driver's license
- Employment with ICON is contingent upon having the legal right to work in the country where the role is based
Additional Requirements
- Legal right to work in the country where the role is based
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