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Cincinnati Children's is a pediatric healthcare and research organization focused on improving children's health through patient care, science, and discovery. The Clinical Research Coordinator III/IV will manage clinical study conduct, regulatory compliance, participant recruitment and retention, communications, and clinical research data management in the Allergy department. Responsibilities Study Conduct/ Clinical

Clinical Research Regulatory Specialist I, Department of Neurology & Rehabilitation Services, Stroke Tags 72 GOOD MATCH Experience Level 100 Skill Industry Exp. 42 Education Higher Education Universities Insider Connection @University of Cincinnati 2 email credits available today Responsibilities Prepares and submits protocol specific documentation to regulatory agencies and internal or external stakeholders includin

Cincinnati Children's is a pediatric healthcare and research organization focused on improving children's health through patient care, science, and discovery. The Clinical Research Coordinator II supports oncology non-therapeutic studies by coordinating study conduct, regulatory documentation, participant recruitment and enrollment, communication, and clinical research data management. Responsibilities Study Conduct/

Responsibilities Demonstrates the ability to develop processes to facilitate implementation of the research protocol to provide effective and safe medical research to all subjects. Demonstrates the ability to identify potential and/or actual issues which may prohibit the accurate implementation of the research protocol and initiate interventions to avoid protocol violations and /or unsafe practice. Demonstrates the a

Medpace is a leading CRO for Biotech companies and we are currently seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team. This role involves managing clinical trials, ensuring timely task delivery, and maintaining project documentation to support the company's success. Responsibilities Engage in clinical trial management on a day to day level Work closely with the project C

Medpace is a full-service clinical contract research organization providing clinical development services to biotechnology, pharmaceutical, and medical device industries. The Clinical Research Project Coordinator will support day-to-day clinical trial management, coordinate project tasks and meetings, maintain reports and timelines, interact with sponsors and study sites, and oversee regulatory filing quality control