Conduct objective clinical research; Manage and ensure integrity of research design, conduct, and reporting; Oversee compliance, financial, and personnel aspects of research projects; Coordinate with necessary departments to ensure research is conducted in accordance with federal regulations and sponsoring agency policy and procedures; Minimize risks to research subjects; Ensure risks are reasonable in relation to anticipated benefits; Ensure equitable selection of human subjects; Obtain informed consent; Monitor data for subject safety; Protect subject privacy and maintain data confidentiality; Include additional safeguards for vulnerable populations; Respond promptly to information requests; Ensure adequate resources and facilities are available; Ensure delegated tasks are performed by qualified personnel; Inform personnel of study procedures, consent requirements, adverse events, and reporting criteria; Conduct research strictly according to the approved protocol; Report deviations; Request approval for protocol modifications; Maintain adequate records; Report adverse events and significant changes in risk/benefit; Provide care for adverse events; Keep subjects informed of new information; Ensure investigators have appropriate credentials and training; Adhere to Good Clinical Practice guidelines; Maintain accurate research subject records; Collaborate with quality and clinical operational oversight.