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We focus on delivering quality and on-time services across a variety of therapeutic indications.\n 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.\nYou will:\nConduct and report all types of onsite monitoring visits\nBe involved in study startup and feasibility research\nPerform CRF review, source document verification and query resolution\nBe responsible for site communication and management\nBe a point of contact for in-house support services and vendors\nCommunicate with internal project teams regarding study progress\nSupport regulatory team in preparing documents for study submissions\n College/University degree in Life Sciences or an equivalent combination of education, training & experience\nIndependent on-site monitoring experience Argentina\nExperience in all types of monitoring visits in Phase II / III\nExperience 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