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PSI CRO

Senior Clinical Research Associate

Vancouver, BC, Canada

$120,000 to $150,000 CAD / year · Full-time

Within 25 km of Coquitlam · About 24.4 km from the city centre

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Job details

Pay: $120,000 to $150,000 CAD / year
Job type: Full-time
Posted: Sep 28, 2026

Original job description

Company Description

PSI is a leading Contract Research Organization with 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 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 SIV, RMV, COV onsite monitoring visits
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
Prepare and particiapte on audits and inspections

Qualifications

College/University degree in Life Sciences or an equivalent combination of education, training & experience
Independent on-site monitoring experience
Experience in all types of monitoring visits in Phase II and/or III
Experience in Oncology is a plus
Full working proficiency in English and French is essential.
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.

Compensation: CAD 120000 - CAD 150000 - yearly

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More about this job

Responsibilities

Conduct and report onsite monitoring visits, review case report forms, verify source documents, resolve queries, and manage communication with clinical sites. Coordinate with internal teams and vendors, support feasibility research and regulatory submissions, and participate in audits and inspections.

Requirements

A college or university degree in life sciences, or an equivalent combination of education, training, and experience, is required, along with independent onsite monitoring experience and experience across monitoring visit types in Phase II and/or III trials. Full working proficiency in English and French, Microsoft Office proficiency, strong planning, communication, collaboration, and problem-solving skills, willingness to travel, and a valid driver’s license are required; oncology experience is an asset.

Skills

Clinical Monitoring
Site Management
Source Document Verification
CRF Review
Query Resolution
Site Communication
Feasibility Research
Regulatory Documentation
Audit Preparation
Inspection Preparation
Oncology
English Proficiency
French Proficiency
Microsoft Office
Planning
Multitasking

Visa sponsorship

Not detected in the job text

Keywords

Clinical Research
Contract Research Organization
Clinical Research Associate
Clinical Trials
Clinical Monitoring
Site Initiation Visit
Routine Monitoring Visit
Close-Out Visit
Case Report Form
Source Document Verification
Query Resolution
Site Management
Feasibility Research
Regulatory Submissions
Audits
Inspections
Phase II
Phase III
Oncology
Life Sciences
Microsoft Office
English
French
Travel
Valid Driver’s License

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