PSI CRO

Global CRO delivering on-time patient enrollment

Senior Clinical Research Associate

Clinical Research OperationsConfirmed live in the last 24 hours

Full-timeToronto, ON, CanadaCA$120k - CA$150k /yr

About the Job

Requirements

A college or university degree in Life Sciences, or an equivalent combination of education, training, and experience.
Experience conducting independent on-site monitoring.
Experience with all types of monitoring visits in Phase II and/or Phase III studies.
Full working proficiency in English.
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 site initiation, routine monitoring, and close-out onsite monitoring visits.
Perform case report form review, source document verification, and query resolution.
Manage site communications and site activities.
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.
Prepare for and participate in audits and inspections.

Desired Qualifications

Experience in Oncology is a plus.

Job Description

We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada:

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.
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

For this position, PSI is not hiring individuals who require work visa sponsorship for employment now or in the future.

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: 120000 to 150000 (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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