Research Coordination: Duties will include performing protocol specific procedures, including lab draws, coordinate with hospital departments for the scheduling of procedures, prep for research visits, instruct participants concerning protocol responsibilities and obtain consent signature. Develop and maintain source documentation, ensure accurate and timely data reporting, and perform quality checks, employ retention strategies to keep enrolled participants engaged in the study, manage data entry in local and central databases, address monitoring and site queries, and inventory supplies as needed.Process Improvement: All members of the study team are expected to contribute to process improvement efforts. This may include identifying solutions to everyday challenges or participating in a process improvement project.Compliance: All members of the study team are responsible for ensuring compliance with federal regulations for human subject research, University policies, and sponsor expectations.Education: All members of the study team are responsible for continuing education relevant to their role. This includes maintaining current human subject research training, attending relevant educational seminars, and professional development in clinical research operations.