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