Act as a Clinical Research Ethicist, providing expertise on the implementation of relevant Human Subjects Protection regulations in clinical research. Conduct regulatory and bioethical reviews of clinical trial protocols, including domestic and international sample and site-specific informed consent documents, for compliance with applicable federal regulations and policies. Carry out literature reviews of ethical codes, regulations, and guidance documents relevant to human subjects' protection in clinical research. Train and supervise staff on application of federal regulations. Develop, review, and update informed consent templates, SOPs, and internal guidelines to promote high quality work product.