Clinical Reseach Associate I

Clinical Research Associate I responsible for monitoring clinical trials and coordinating all activities for setting up and monitoring a study, including completing accurate study status reports, maintaining study documentation, efficiently running sponsor-generated queries, and ensuring patient safety and regulatory compliance. The role emphasizes developing and maintaining strong, collaborative relationships with clinical investigators and site staff, and participating in preparation/review of study documentation and feasibility studies for new proposals. Requires independent coordination of monitoring activities and travel (~60%) to sites as needed, with an applicant based in Argentina (Buenos Aires).