JOB DESCRIPTION
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 agile 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.

📌 PSI CRO is hiring: Senior Clinical Research Associate in Vancouver
🏢 PSI CRO
📍 Vancouver