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.