Job DescriptionIf you are currently a CRA I looking forward to the next step of your career, this might be the right position for you!
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:Conduct and report all types of onsite monitoring visitsBe involved in study startup and feasibility researchPerform CRF review,



source document verification and query resolutionBe responsible for site communication and managementBe a point of contact for in-house support services and vendorsCommunicate with internal project teams regarding study progressSupport regulatory team in preparing documents for study submissionsQualificationsCollege/University degree in Life Sciences or an equivalent combination of education, training & experience 1 - 2 years of independent on-site monitoring experience in Argentina Experience in all types of monitoring visits in Phase II / III Full working proficiency in English and Spanish Proficiency in MS Office applications Ability to plan and work in a dynamic team environment Communication, collaboration, and problem-solving skills Ability to travelAdditional InformationThis 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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📌 Clinical Research Associate Ii. (Buenos Aires)
🏢 PSI
📍 Buenos Aires