Clinical Research Associate
Current• Monitor NIH intramural and extramural multi-institutional research protocols to ensure clinical trials are conducted in a timely manner.• Provide quality control of data, ensuring compliance with regulatory requirements and study protocols.• Assist in the design, preparation, and coordination of research projects and clinical trials.• Collect, process, and maintain research data and patient information, ensuring confidentiality and compliance with ethical standards.• Prepare and maintain forms and documents, including consent forms, case report forms, and regulatory documents.