Compensation: CAD 120,000 - CAD 150,000 - yearly
Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global, mid-size company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Job Description We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada:
Conduct and reportSIV, RMV,COVonsite 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
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 This is a great chance for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

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