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 outstanding opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

📌 Senior Clinical Research Associate (Vancouver)
🏢 PSI CRO
📍 Vancouver