Senior CRA
psicro
Posted: March 17, 2026
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Quick Summary
We are seeking a Clinical Research Associate to join our team in Vancouver, Canada, as a Senior CRA. As a key member of our team, you will be responsible for conducting and reporting on-site monitoring visits and performing CRF reviews. You will work closely with our research team to deliver high-quality studies that meet our clients' needs.
Required Skills
Job 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.
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
 
• 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
 
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.