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The Clinical Research Associate will conduct onsite monitoring visits, perform CRF reviews, and manage site communications to ensure study quality. They will also support regulatory teams with document preparation and participate in feasibility research and audits.
PSI is a leading Contract Research Organization with more than 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:
What We Offer:
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
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