Clinical Research Coordinator

54-62K, possible 2k incentive, excellent benefits

Houston, TX

Candidates must have clinical research experience. 

• Provide study coordination including screening of potential patients for protocol eligibility and participation in the informed consent process
• Responsible for accurate and timely source documents, data collection, documentation, entry and reporting, including timely response to sponsor queries
• Responsible for compiling and reporting on each study including information related to protocol activity, workload and other research information, present this information at regular research staff meetings
• Informing participants about study objectives
• Monitoring research participants to ensure adherence to study rules
• Adhering to research regulatory standards and ethical standards
• Ensuring that the necessary supplies and equipment for a study are in stock and in working order
• Engaging with subjects and understanding their concerns