Clinical Research Associate II
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About the role
Remote Clinical Research Associate II role with PSI, based in Toronto, supporting clinical studies across therapeutic indications. Responsibilities include onsite monitoring visits, study startup, CRF review, source document verification, query resolution, site and vendor management, feasibility work, and regulatory submission support. Requires a Life Sciences college/university degree or equivalent education, training and experience; independent North American monitoring experience; Phase II/III monitoring experience; English and French proficiency; travel ability; and a valid driver’s license.
Key requirements
- • College/University degree in Life Sciences or an equivalent combination of education, training & experience
- • Required skills: Independent on-site monitoring experience in North America, Experience in all types of monitoring visits in Phase II and/or III, Clinical study startup, CRF review, Source document verification, Query resolution, Site communication and management, Vendor coordination, Study progress communication, Feasibility research, Regulatory submission document preparation, MS Office applications, Planning and multitasking, Communication, Collaboration, Problem-solving, Ability to travel
- • Required languages: English, French
- • Professional registration/licence
Opportunity details
- • Workplace: Remote
- • Posted: Oct 23, 2026
- • Original advert language: English
Full vacancy
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See original vacancy ↗Employer’s role description
Job title: Clinical Research Associate II
Location: Toronto, ON, Canada
Employment type: Full-time
Compensation: CAD 98000 - CAD 120000 - yearly
Workplace type: Remote
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.
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
- 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.
Verification
- ✓ Employer verification
- ✓ Original posting located
- Last verified: Oct 24, 2026