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The Clinical Research Associate will conduct onsite monitoring visits, manage site communications, and ensure data quality and compliance with study protocols. They will also support study startup activities, regulatory submissions, and oversee project timelines and schedules.
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 Contract Clinical Research Associate II, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.
Home-based (freelance)
You will:
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