Job Summary: Join Medpace at our Sao Paulo office! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Trial Assistant to join our LatAm Site Contract Team within the Clinical
Job Summary: Join Medpace at our Sao Paulo office! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Contract Specialist to join our LatAm Site Contract Team within the Clinical Operations team. This
Job Summary: Responsibilities: - Responsible for the distribution of safety reports to regulatory authorities; - Create and maintain project-related trackers and status reports; - Distribute and track safety-related notifications; - Conduct quality control reviews of departmental
Job Summary: Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and
Job Summary: As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining vital experience in study start up. You will be a productive member of
Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Sao Paulo, Brazil . Our therapeutic
Job Summary: As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining vital experience in study start up. You will be a productive member of