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 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.
Proficiency in MS Office applications
Ability to plan, multitask and work in a dynamic team setting
Communication, collaboration, and problem-solving skills
Ability to travel
Valid driver’s license
Additional Information
For this position, PSI is not hiring individuals who require work visa sponsorship for employment now or in the future.
This is a excellent prospect for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
📌 Senior Clinical Research Associate Toronto (Canada)
🏢 PSI CRO
📍 Canada
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