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