PSI CRO

Global CRO delivering on-time patient enrollment

Clinical Research Associate 2

Clinical Research OperationsConfirmed live in the last 24 hours

Full-timeQuébec City, QC, CanadaCA$98k - CA$120k /yr

About the Job

Requirements

A college or university degree in Life Sciences, or an equivalent combination of education, training, and experience.
Independent on-site monitoring experience in North America.
Experience conducting all types of monitoring visits in Phase II and/or III studies.
Full working proficiency in English and French.
Proficiency in Microsoft Office applications.
Ability to plan and multitask in a dynamic team environment.
Communication, collaboration, and problem-solving skills.
Ability to travel.
A valid driver's license.

Responsibilities

Conduct and report all types of on-site monitoring visits.
Participate in study start-up, if applicable.
Perform case report form review, source document verification, and query resolution.
Manage site communications and site operations.
Serve as a point of contact for in-house support services and vendors.
Communicate study progress to internal project teams.
Participate in feasibility research.
Support the regulatory team in preparing documents for study submissions.

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.

Compensation: 98000 to 120000 (CAD) (YEARLY)

About the Company

PSI CRO

Global CRO delivering on-time patient enrollment

PSI CRO is a global contract research organization that handles clinical trials for multiple therapeutic areas, with a focus on enrolling patients on schedule and delivering studies on time. Its services span feasibility assessments, trial planning, site selection, patient recruitment, and multi-continent trial execution across 50+ countries, backed by medical doctor resources dedicated to accurate timeline predictions. Unlike many CROs, PSI emphasizes predictable enrollment and on-time project delivery, aiming for high client satisfaction and repeat business through a pragmatic, no-nonsense approach. The company’s goal is to be regarded as the best CRO in the world by both clients and employees, achieved through reliable timelines, strong execution, and low staff turnover.

Company size: 1,001-5,000
Company stage: Not listed
Total funding: Not listed
Headquarters: Switzerland
Founded: 1995

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