• Conduct clinical trials related to transplant immunology and virology with a focus on the treatment of hepatitis C and B.• Develop, negotiate, and monitor research protocol budgets. • Complete billing forms for all study related procedures according to ICD-9, CPT-4, and HCPCS codes.• Recruit, screen, enroll, and obtain consent from clinical trial participants. • Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments, and maintaining contact with study participants.• Assure compliance with all relevant IRB and other regulatory agency requirements.• Assist in the preparation of IRB documents and reports.• Work with the Principal Investigator to develop, implement, and maintain comprehensive databases and files related to the program.• Conduct initiation site visits, maintain quality of case report forms, process and ship laboratory specimens, and assist in the development of clinical trial budgets.

• Provided supervision, direction, and training for research nurses within the Division of Transplantation.• Developed and maintained a clinical research database of liver transplant patients utilizing SPSS format.• Performed data statistical analysis for the purpose of department quality improvement activities.• Coordinated all department research activities including clinical trials, abstracts, publications, and presentations. • Participated in all aspects of project planning and budgeting.• Implemented clinical research protocols in accordance with institutional standard operating practices, FDA regulations, and GCP guidelines.