Maintain extensive knowledge of the STVHCS, Immunosuppression Clinic (ISC) research protocols; develop recruitment methods for patients to participate in studies; screen patients to determine study eligibility by reviewing patient medical information or interviewing subjects after subject expresses potential interest and with primary care provider support of enrollment; perform consent process and obtain informed consent from research subjects; initiate submission of regulatory documents to Veteran Affairs Research & Development (VA R&D), Institutional Review Board (IRB), and sponsor in a timely manner; contact patients for appointment confirmations and scheduling purposes; provide education and instruction of study medication use, administration, storage, side effects and monitoring for adverse drug reactions; provide education regarding study activities to patients, relatives and medical center staff as necessary per protocol; conduct study visits with subjects; demonstrate proficiency with computerized patient record system (CPRS) by documenting visits and correspondence in progress notes; schedule subject visits through U.S. Government computer system (VISTA), complete case report forms (CRF) and other forms as required by protocol, with completion in a timely fashion; maintain complete and accurate data collection and source documents; obtain and organize data such as tests results, diaries/cards, or other necessary information for the study; inform immediately the Principal Investigator (PI) in the case of any significant or serious adverse event occurring to a patient enrolled in a study with additional reporting to IRB and the study sponsor; collect and handle various types of human specimens; IATA certified to ship hazardous and dangerous goods; perform phlebotomy to obtain subject specimens as required per protocol; process and store specific specimens per protocol; conduct quality management review of currently enrolled study subjects; maintain regulatory binders in compliance with Good Clinical Practices; access confidential medical and personal information in accordance with the Healthcare Insurance Portability and Accountability Act (HIPAA); participate in continuing education programs, seminars and workshops to keep abreast of the clinical area of HIV infection and related research; and perform other duties as assigned.