Clinical Research Associate II
At PSI CRO · Toronto, ON, Canada
- Full-time
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Where you can work from
Open to Canada
“Toronto, ON, Canada”
From the location.
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- Posted
- 11 hours ago
- First seen by us
- 24 October 2026
- Last checked
- 8 hours ago
Job description
From PSI CRO’s job post, as they wrote it.
Job Description
As a Clinical Research Associate II at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.
You will:
* Conduct and report all types of onsite monitoring visits
* Be involved in study startup (if applicable)
* Perform CRF review, source document verification and query resolution
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* Be responsible for site communication and management
* Be a point of contact for in-house support services and vendors
* Communicate with internal project teams regarding study progress
* Participate in feasibility research
* Support regulatory team in preparing documents for study submissions
Qualifications
* College/University degree in Life Sciences or an equivalent combination of education, training & experience
* Independent on-site monitoring experience in North America.
* Experience in all types of monitoring visits in Phase II and/or III
* Full working proficiency in English and French.
* Proficiency in MS Office applications
* Ability to plan, multitask and work in a dynamic team environment
* Communication, collaboration, and problem-solving skills
* Ability to travel
* Valid driver’s license
Additional Information
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
Company Description
PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
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