Company 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.
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:
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Conduct and report SIV, RMV, COV onsite monitoring visits
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Perform CRF review, source document verification and query resolution
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Be responsible for site communication and management
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Be a point of contact for in-house support services and vendors
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Communicate with internal project teams regarding study progress
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Participate in feasibility research
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Support regulatory team in preparing documents for study submissions
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Prepare and particiapte on audits and inspections
Qualifications
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College/University degree in Life Sciences or an equivalent combination of education, training & experience
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Independent on-site monitoring experience
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Experience in all types of monitoring visits in Phase II and/or III
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Experience in Oncology is a plus
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Full working proficiency in English and French is essential.
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Proficiency in MS Office applications
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Ability to plan, multitask and work in a dynamic team environment
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Communication, collaboration, and problem-solving skills
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Ability to travel
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Valid driver’s license
Additional Information
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
